Provided is a process for recovery of a functionalized compound reaction product comprising contacting (i) an oxidizing electrophile comprising a main group element, and (ii) a compound comprising at least one CH bond, in an acidic medium to form a reaction milieu comprising a functionalized compound reaction product, contacting the reaction milieu with a water-immiscible organic solvent, separating the water-immiscible organic solvent from the reaction milieu, wherein the functionalized compound reaction product is dissolved in the water-immiscible organic solvent, and separating the functionalized compound reaction product and the water-immiscible organic solvent. The water-immiscible extraction solvent can be the same compound as the compound comprising as least one CH bond, for example, propane or n-butane.

Provided is a process for recovery of a functionalized compound reaction product comprising contacting (i) an oxidizing electrophile comprising a main group element, and (ii) a compound comprising at least one CH bond, in an acidic medium to form a reaction milieu comprising a functionalized compound reaction product, contacting the reaction milieu with a water-immiscible organic solvent, separating the water-immiscible organic solvent from the reaction milieu, wherein the functionalized compound reaction product is dissolved in the water-immiscible organic solvent, and separating the functionalized compound reaction product and the water-immiscible organic solvent. The water-immiscible extraction solvent can be the same compound as the compound comprising as least one CH bond, for example, propane or n-butane.

The invention relates to a method for producing 1,3-butanediene from a butanediol feedstock that includes: a) A step for esterification of butanediol by a carboxylic acid to form the corresponding diester; b) A step for pyrolysis of the diester effluent obtained from step a); c) A step for distillation fed by at least the carboxylic acid effluent obtained from step a), and producing an aqueous distillate and a carboxylic acid residue; d) A step for drying the carboxylic acid that is fed at least by the carboxylic acid residue obtained from step c) and producing a water effluent and a carboxylic acid product that feeds step a).

The invention relates to a method for producing 1,3-butanediene from a butanediol feedstock that includes: a) A step for esterification of butanediol by a carboxylic acid to form the corresponding diester; b) A step for pyrolysis of the diester effluent obtained from step a); c) A step for distillation fed by at least the carboxylic acid effluent obtained from step a), and producing an aqueous distillate and a carboxylic acid residue; d) A step for drying the carboxylic acid that is fed at least by the carboxylic acid residue obtained from step c) and producing a water effluent and a carboxylic acid product that feeds step a).

The invention relates to a method for producing 1,3-butanediene from a butanediol feedstock that includes: a) A step for esterification of butanediol by a carboxylic acid to form the corresponding diester; b) A step for pyrolysis of the diester effluent obtained from step a); c) A step for distillation fed by at least the carboxylic acid effluent obtained from step a), and producing an aqueous distillate and a carboxylic acid residue; d) A step for drying the carboxylic acid that is fed at least by the carboxylic acid residue obtained from step c) and producing a water effluent and a carboxylic acid product that feeds step a).

Provided is a process for the preparation of certain 1,4-bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst comprising a palladium compound to afford certain oxo-substituted bicyclo[2.2.2]octane species. The process of the invention thus affords a novel and simplified means for the commercial production of a wide variety of bicyclo[2.2.2]octane derivatives.

Provided is a process for the preparation of certain 1,4-bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst comprising a palladium compound to afford certain oxo-substituted bicyclo[2.2.2]octane species. The process of the invention thus affords a novel and simplified means for the commercial production of a wide variety of bicyclo[2.2.2]octane derivatives.

A method of selective conversion of Abienol, represented by formula 1, to Sclareodiol, represented by formula 2 ##STR00001##
by ozonolysis and subsequent reduction. The ozonolysis is carried out at temperatures above 60 C., preferably in nonhalogenated solvents. R is selected from H, acetals, aminals, optionally substituted alkyl groups, such as benzyl group, carboxylates such as acetates or formates, carbonates such as methyl or ethyl carbonates, carbamates, and any protecting group which can be attached to 1 and cleaved from 2, R is selected from CHCH.sub.2, an alkyl moiety with C2-C20, e.g. CH.sub.2CH.sub.3, or a cycloalkyl or polycycloalkyl moiety with C3-C20, e.g. cyclopropyl, optionally alkylated, respectively, and the wavy bond is depicting an unspecified configuration of the adjacent double bond between C2 and C3.

A method of selective conversion of Abienol, represented by formula 1, to Sclareodiol, represented by formula 2 ##STR00001##
by ozonolysis and subsequent reduction. The ozonolysis is carried out at temperatures above 60 C., preferably in nonhalogenated solvents. R is selected from H, acetals, aminals, optionally substituted alkyl groups, such as benzyl group, carboxylates such as acetates or formates, carbonates such as methyl or ethyl carbonates, carbamates, and any protecting group which can be attached to 1 and cleaved from 2, R is selected from CHCH.sub.2, an alkyl moiety with C2-C20, e.g. CH.sub.2CH.sub.3, or a cycloalkyl or polycycloalkyl moiety with C3-C20, e.g. cyclopropyl, optionally alkylated, respectively, and the wavy bond is depicting an unspecified configuration of the adjacent double bond between C2 and C3.

Cannabidiolic acid esters, compositions comprising them and uses thereof in the treatment of various diseases, conditions and symptoms.