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HRID 131773作成日:2026年10月26日

Vinyl benzoate → Acetate

https://huagongshe.com/reaction/131773

反応式

関与物質

役割名称HCID仕込み量
反応物Vinyl benzoateHCID 13037—
溶媒tert-Butyl methyl etherHCID 15413—
生成物AcetateHCID 175—
生成物FormateHCID 283—
生成物ButyrateHCID 104775—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384980B2
出典データセットuspto-grants-2008_06
ORD IDord-d06c334624a346fd8129495d47d93ed1
出典メモuspto-grants-2008_06