A polyisobutylene-substituted hydroxyaromatic compound and derivatives thereof which are suitable for use as additives in lubricating compositions. The polyisobutylene-substituted hydroxyaromatic compound may include the reaction product of a hydroxyaromatic compound with a polyisobutylene having a number average molecular weight of 150 to 800.

A polyisobutylene-substituted hydroxyaromatic compound and derivatives thereof which are suitable for use as additives in lubricating compositions. The polyisobutylene-substituted hydroxyaromatic compound may include the reaction product of a hydroxyaromatic compound with a polyisobutylene having a number average molecular weight of 150 to 800.

This disclosure provides 8,9-dihydrocannabinoid derivatives, deuterated cannabinoid derivatives, and tritiated cannabinoid derivatives. The disclosure also provides compositions, methods of use, and processes of preparation of the foregoing derivatives.

This disclosure provides 8,9-dihydrocannabinoid derivatives, deuterated cannabinoid derivatives, and tritiated cannabinoid derivatives. The disclosure also provides compositions, methods of use, and processes of preparation of the foregoing derivatives.

Herein are described apparatus and processes for the preparation of cannabinoids, such as cannabidiol (CBD) and derivatives thereof. The apparatus and processes described can be used for the one-step, flow-mediated synthesis of cannabidiol and derivatives with improved overall yield, material throughput, and product purity relative to batch processes.

Herein are described apparatus and processes for the preparation of cannabinoids, such as cannabidiol (CBD) and derivatives thereof. The apparatus and processes described can be used for the one-step, flow-mediated synthesis of cannabidiol and derivatives with improved overall yield, material throughput, and product purity relative to batch processes.

A phenol alkylation catalyst exhibiting a desirable combination of activity, selectivity, and regenerability is prepared from a catalyst precursor that includes specific amounts of magnesium oxide, copper oxide or a copper oxide precursor, a hydrous magnesium aluminosilicate-containing binder, a pore-former, a lubricant, and water. Methods of forming and regenerating the catalyst, as well as a phenol alkylation method, are described.

A phenol alkylation catalyst exhibiting a desirable combination of activity, selectivity, and regenerability is prepared from a catalyst precursor that includes specific amounts of magnesium oxide, copper oxide or a copper oxide precursor, a hydrous magnesium aluminosilicate-containing binder, a pore-former, a lubricant, and water. Methods of forming and regenerating the catalyst, as well as a phenol alkylation method, are described.

A phenol alkylation catalyst exhibiting a desirable combination of activity, selectivity, and regenerability is prepared from a catalyst precursor that includes specific amounts of magnesium oxide, copper oxide or a copper oxide precursor, a hydrous magnesium aluminosilicate-containing binder, a pore-former, a lubricant, and water. Methods of forming and regenerating the catalyst, as well as a phenol alkylation method, are described.

Herein are described apparatus and processes for the preparation of cannabinoids, such as cannabidiol (CBD) and derivatives thereof. The apparatus and processes described can be used for the one-step, flow-mediated synthesis of cannabidiol and derivatives with improved overall yield, material throughput, and product purity relative to batch processes.