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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55422Generated: October 29, 2026

Ethyl Acetate → HCID 67661107, compound

https://huagongshe.com/reaction/55422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant(3aRS,6SR,7aSR)-6-acetoxymethyl-2-benzyl-4-perhydroisoindoloneHCID 18931543—
ReactantHCID 178489560HCID 178489560—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67661107HCID 6766110737.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a suspension of 2-methoxyphenylmagnesium bromide (prepared from 24.9 cm3 of 2-bromoanisole and 4.86 g of magnesium) in 200 cm3 of anhydrous tetrahydrofuran is added a solution of 8.0 g of (3aRS,6SR,7aSR)-6-acetoxymethyl-2-benzyl-4-perhydroisoindolone in 60 cm3 of anhydrous tetrahydrofuran. The reaction mixture is stirred for 20 hours at 20° C. and then cooled to +5° C. and treated with 120 cm3 of saturated aqueous ammonium chloride solution and 100 cm3 of ethyl acetate. After filtration of the mixture, the organic phase is washed with brine and then dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of silica gel (particle size 0.06-0.200 mm, height 40 cm) in a mixture of 1,2-dichloroethane and methanol (95/5 by volume). After recrystallization in ethyl ether, 3.2 g of (3aRS,4RS,6SR, 7aSR)-2-benzyl-6-hydroxymethyl-4-(2-methoxyphenyl)-4-perhydroisoindolol are obtained, in the form of a white solid melting at 110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624950
Source datasetuspto-grants-1997_04
ORD IDord-204dd5be0eb74850b27ab41998e173e3
Source noteuspto-grants-1997_04