The present disclosure describes methods for silylating aromatic organic substrates, and associated chemical systems, said methods comprising or consisting essentially of contacting the aromatic organic substrate with a mixture of (a) at least one organosilane and (b) at least one strong base, under conditions sufficient to silylate the aromatic substrate.

The present disclosure describes methods for silylating aromatic organic substrates, and associated chemical systems, said methods comprising or consisting essentially of contacting the aromatic organic substrate with a mixture of (a) at least one organosilane and (b) at least one strong base, under conditions sufficient to silylate the aromatic substrate.

Purified and modified Cannabis products and methods for producing the same. The purified Cannabis product comprises substantially no volatile organic compounds while retaining Total Potential cannabinoid content. The modified Cannabis product comprises a purified Cannabis product modified by at least one added volatile unsaturated hydrocarbon. The modified Cannabis product is formed by extracting a volatile organic compound from a Cannabis raw material to form a purified Cannabis product, and then adding the at least one volatile unsaturated hydrocarbon to the purified Cannabis product to form the modified Cannabis product and cause an enhanced user experience during combustion and inhalation of the modified Cannabis product.

The invention relates to a process for preparing a specific hydroxy compound by means of decarboxylation of a specific carboxylic acid compound or a salt of said carboxylic acid compound, to a method for preparing a diaryl carbonate, a bisphenol or a polycarbonate, a diaryl carbonate or bisphenol, a polycarbonate, and to a method for adjusting the isotope ratio of C14 to C12 in a polymer. A specific solvent is used during decarboxylation.

The invention relates to a process for preparing a specific hydroxy compound by means of decarboxylation of a specific carboxylic acid compound or a salt of said carboxylic acid compound, to a method for preparing a diaryl carbonate, a bisphenol or a polycarbonate, a diaryl carbonate or bisphenol, a polycarbonate, and to a method for adjusting the isotope ratio of C14 to C12 in a polymer. A specific solvent is used during decarboxylation.

The invention relates to a process for preparing a specific hydroxy compound by means of decarboxylation of a specific carboxylic acid compound or a salt of said carboxylic acid compound, to a method for preparing a diaryl carbonate, a bisphenol or a polycarbonate, a diaryl carbonate or bisphenol, a polycarbonate, and to a method for adjusting the isotope ratio of C14 to C12 in a polymer. A specific solvent is used during decarboxylation.

Processes for making phenol and xylenes from a phenols-containing feed are described. The processes involve transalkylation of alkylphenols to form phenol and alkylbenzenes. The phenol is separated from the alkylbenzenes, and the alkylbenzenes may be separated into benzene, toluene, xylenes, and heavy alkylbenzene streams. The benzene stream may be recycled to the transalkylation reaction zone. The toluene may be sent to a disproportionation reaction zone, and the product is sent back to the aromatic separation zone. The toluene can also be recycled to the transalkylation zone. The xylenes are separated into a p-xylene stream and a mixed xylene stream comprising m-xylene and o-xylene. The mixed xylene stream is isomerized and the isomerized product is sent back to the aromatic separation zone. The heavy alkylbenzenes are dealkylated and separated, with the aromatic stream being recycled to the aromatic separation zone.

Processes for making phenol and xylenes from a phenols-containing feed are described. The processes involve transalkylation of alkylphenols to form phenol and alkylbenzenes. The phenol is separated from the alkylbenzenes, and the alkylbenzenes may be separated into benzene, toluene, xylenes, and heavy alkylbenzene streams. The benzene stream may be recycled to the transalkylation reaction zone. The toluene may be sent to a disproportionation reaction zone, and the product is sent back to the aromatic separation zone. The toluene can also be recycled to the transalkylation zone. The xylenes are separated into a p-xylene stream and a mixed xylene stream comprising m-xylene and o-xylene. The mixed xylene stream is isomerized and the isomerized product is sent back to the aromatic separation zone. The heavy alkylbenzenes are dealkylated and separated, with the aromatic stream being recycled to the aromatic separation zone.

Processes for making phenol and xylenes from a phenols-containing feed are described. The processes involve transalkylation of alkylphenols to form phenol and alkylbenzenes. The phenol is separated from the alkylbenzenes, and the alkylbenzenes may be separated into benzene, toluene, xylenes, and heavy alkylbenzene streams. The benzene stream may be recycled to the transalkylation reaction zone. The toluene may be sent to a disproportionation reaction zone, and the product is sent back to the aromatic separation zone. The toluene can also be recycled to the transalkylation zone. The xylenes are separated into a p-xylene stream and a mixed xylene stream comprising m-xylene and o-xylene. The mixed xylene stream is isomerized and the isomerized product is sent back to the aromatic separation zone. The heavy alkylbenzenes are dealkylated and separated, with the aromatic stream being recycled to the aromatic separation zone.

A process for manufacturing Pure Propofol with a purity of more than 99.90% is disclosed, said process comprising dissolving Crude Propofol in a solvent in which it is soluble to form a solution, treating the solution with aqueous alkali to form an aqueous alkali layer and a solvent layer, separating the aqueous alkali layer from the solvent layer using a phase separation technique, distilling off the solvent from the solvent layer, and distilling a residue of the solvent containing Propofol using steam or boiling water in a presence of dilute alkali and antioxidant like metabisulfite, under normal pressure or mild vacuum.