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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55402생성일: 2026년 10월 24일

Ammonium Chloride → (3aRS,4RS,5RS,7aSR)-2-benzyl-4-(2-methoxyphenyl)-4,5-perhydroisoindolediol

https://huagongshe.com/ko/reaction/55402

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물(3aRS,5RS,7aSR)-5-acetoxy-2-benzyl-4-perhydroisoindoloneHCID 67714196—
반응물HCID 178489560HCID 178489560—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물(3aRS,4RS,5RS,7aSR)-2-benzyl-4-(2-methoxyphenyl)-4,5-perhydroisoindolediolHCID 6771392926.8%

반응 단계

To a suspension of 27.6 g of 2-methoxyphenylmagnesium bromide in 60 cm' of tetrahydrofuran are added dropwise, at room temperature and with stirring, a solution of 4.7 g of (3aRS,5RS,7aSR)-5-acetoxy-2-benzyl-4-perhydroisoindolone in 90 cm3 of tetrahydrofuran. The reaction mixture is stirred at room temperature for 3 hours, treated with 200 cm3 of saturated aqueous ammonium chloride solution and taken up in 200 cm3 of ethyl ether and 100 g of ice. The organic phase is separated out after settling has taken place, dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa). The residue is crystallized in 80 cm3 of petroleum ether and then chromatographed on a column of silica gel (particle size 0.04-0.06 mm, diameter 1 cm, height 20 cm), eluting under a pressure of 0.5 bar of nitrogen with a mixture of dichloromethane and methanol (95/5 by volume) and collecting 25 cm3 fractions. Fractions 14 to 21 are combined and then concentrated to dryness under reduced pressure (2.5 kPa). 1.55 g of (3aRS,4RS,5RS,7aSR)-2-benzyl-4-(2-methoxyphenyl)-4,5-perhydroisoindolediol are obtained, melting at 140° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624950
출처 데이터셋uspto-grants-1997_04
ORD IDord-67d3926d58e94c3b98873508a730e72e
출처 메모uspto-grants-1997_04