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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196285Generated: October 31, 2026

Phenylacetyl chloride → HCID 86745796, compound

https://huagongshe.com/reaction/1196285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
Reactant136916-30-8HCID 67916164—
SolventDichloromethaneHCID 6344—
ProductHCID 86745796HCID 86745796—

Reaction Steps

Phenylacetyl chloride (0.82 cc) is added to a solution, cooled to +5° C., of 7,7-diphenyl-2,3,3a,4,7,7a-hexahydro-1H-isoindol-4-one hydrochloride (2 g) and triethylamine (1.7 cc) in dry dichloromethane (20 cc). The reaction mixture is stirred for 1 hour at +5° C. and for 1 hour at room temperature; it is washed with distilled water (2×20 cc), dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa). The residue is crystallized in acetonitrile (15 cc). The crystals are drained, washed with isopropyl ether (10 cc), dried and then recrystallized in acetonitrile (20 cc). The crystals obtained are drained and dried. (3aRS, 7aRS)-7,7a-Diphenyl-2-(phenylacetyl)-2,3,3a,4,7,7a-hexahydro-1H-isoindol-4-one (2.7 g), m.p. 188° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112988
Source datasetuspto-grants-1992_05
ORD IDord-b741b008992245e9a3ccabd98c897528
Source noteuspto-grants-1992_05