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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322877생성일: 2026년 10월 25일

Sodium hydride → ethyl (RS)-4-(2-methoxycarbonyl-5-benzyloxyphenoxy)-4-phenylbutanoate

https://huagongshe.com/reaction/322877

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Methyl 4-(benzyloxy)-2-hydroxybenzoateHCID 225489—
반응물Ethyl 4-chloro-4-phenylbutanoateHCID 12847348—
용매DimethylformamideHCID 6228—
생성물ethyl (RS)-4-(2-methoxycarbonyl-5-benzyloxyphenoxy)-4-phenylbutanoateHCID 2320431057.6%

반응 단계

A stirred suspension of sodium hydride (340 mg) in dry dimethylformamide (100 mL) is treated portionwise with methyl 4-benzyloxy-2-hydroxybenzoate (2 g). After stirring at ambient temperature for 30 minutes, it is treated with ethyl (RS)-4-chloro-4-phenylbutanoate (1.9 g) in one portion and stirred for 16 hours at ambient temperature, and then for two hours at 80° C. The reaction mixture is then concentrated in vacuo and the residue is partitioned between ethyl acetate (100 mL) and water (100 mL). The organic layer is dried over magnesium sulphate, filtered and concentrated in vacuo. Flash chromatography of the resulting oil, eluting with 5-10% ethyl acetate/cyclohexane, affords ethyl (RS)-4-(2-methoxycarbonyl-5-benzyloxyphenoxy)-4-phenylbutanoate (2 g), in the form of a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211234B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-7554c6594e5140b6b1022816babaec49
출처 메모uspto-grants-2001_04