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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029948Generated: October 30, 2026

Phenylacetyl chloride → HCID 67916020, compound

https://huagongshe.com/reaction/1029948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
ReactantHCID 67915919HCID 67915919—
SolventDichloromethaneHCID 6344—
ProductHCID 67916020HCID 6791602020.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

A suspension of (3aRS,7aRS)-7,7-bis-(3-tolyl)-4-perhydroisoindolone hydrochloride (1.5 g) in dichloromethane (30 cc) cooled to +4° C. is treated with triethylamine (1.15 cc) and then with phenylacetyl chloride (0.63 g). The reaction mixture is stirred for 5 hours at 25° C. and then washed with water (3×100 cc). The organic phase is dried over magnesium sulphate and filtered and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is crystallized twice from acetonitrile to give (3aRS,7aRS)-7,7-bis-(3-tolyl)-2-(phenylacetyl)-4-perhydroisoindolone (0.36 g). m.p.=207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102667
Source datasetuspto-grants-1992_04
ORD IDord-d9e78980a31749f582720bbe11a8cc45
Source noteuspto-grants-1992_04