Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131773Generated: October 26, 2026

Vinyl benzoate → Acetate

https://huagongshe.com/reaction/131773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl benzoateHCID 13037—
Solventtert-Butyl methyl etherHCID 15413—
ProductAcetateHCID 175—
ProductFormateHCID 283—
ProductButyrateHCID 104775—

Reaction Steps

A mixture consisting of Intermediate B (80 mg, 0.23 mmol), vinyl ester (0.4 ml), tert.-butyl methylether (18 ml), and lipase enzyme (1.0 g) was gently shaken at room temperature. Benzylic formate, acetate, and n-butyrate were prepared from the corresponding vinyl ester donors using SAM I lipase (Amano Pharmaceutical Co.). Benzoylation was achieved with vinyl benzoate in the presence of Lipozym IM 20 (Novo Nordisk), whereas pivalates and isobutyrates were obtained from the corresponding vinyl esters under catalysis of Novozym SP 435 (Novo Nordisk). Tlc analysis indicated after 2-24 hrs complete disappearence of the starting material (Rf=0.45 (3)). The mixture was filtered and then evaporated under high vacuum (<40° C.) to give the carboxylic acid (R1—CO2H) salts of the respective benzylic monoesters as colourless to light yellow oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384980B2
Source datasetuspto-grants-2008_06
ORD IDord-d06c334624a346fd8129495d47d93ed1
Source noteuspto-grants-2008_06