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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196232Generated: October 25, 2026

Diisopropyl Ether → (3aRS,7aRS)-7,7-Diphenyl-2-vinyloxycarbonylperhydro-4-isoindolone

https://huagongshe.com/reaction/1196232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantVinyl chloroformateHCID 78808—
Reactant(3aRS, 7aRS)-2-benzyl-7,7-diphenyl-4-perhydroisoindoloneHCID 19384608—
Solvent1,2-DichloroethaneHCID 11—
Product(3aRS,7aRS)-7,7-Diphenyl-2-vinyloxycarbonylperhydro-4-isoindoloneHCID 67915936—

Reaction Steps

Vinyl chloroformate (56 cc) is added dropwise in the course of 10 minutes to a solution, cooled to +5° C., of (3aRS,7aRS)-2-benzyl-7,7-diphenylperhydro-4-isoindolone (193 g) in 1,2-dichloroethane (1225 cc). After stirring for 30 minutes at between 10° and 20° C., the reaction mixture is heated to reflux for 90 minutes, cooled and concentrated to dryness under reduced pressure (2.7 kPa then 1 kPa). The crystalline mass obtained is stirred vigorously with cold isopropyl ether (200 cc). The crystals obtained are drained, washed with isopropyl ether (2×100 cc) and dried. (3aRS,7aRS)-7,7-Diphenyl-2-vinyloxycarbonylperhydro-4-isoindolone (177 g), m.p. 178° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112988
Source datasetuspto-grants-1992_05
ORD IDord-fb4d8ce5e2b04fd1addfd5c8b9ceaa30
Source noteuspto-grants-1992_05