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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 343304생성일: 2026년 10월 25일

Formic Acid → 2-Formyl-17beta-estradiol

https://huagongshe.com/reaction/343304

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물Sodium hydrideHCID 24758—
반응물Chlorosulfonyl isocyanateHCID 70918—
반응물17beta-Tert-butyldimethylsilyloxy-3-hydroxyestra-1,3,5(10)-triene-2-carboxaldehydeHCID 54522215—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-Formyl-17beta-estradiolHCID 999498018.3%

반응 단계

To a solution of chlorosulfonyl isocyanate (0.13 mL, 1.5 mmol) in CH2Cl2 (1.0 mL) was added formic acid (0.31 mL of a CH2Cl2 solution, 5.0M, 1.6 mmol) at 0° C. The reaction mixture was warmed to room temperature and stirred for 1 h. To a solution of 17β-tert-butyldimethylsilyloxy-3-hydroxyestra-1,3,5(10)-triene-2-carbox aldehyde (9, 0.129 g, 0.31 mmol) in DMF (3.0 mL) was added sodium hydride (0.044 g of a mineral oil dispersion, 60%, 1.1 mmol) at 0° C. The reaction mixture was stirred for 1 h, the pre-prepared reagent was added, and stirring continued for 4 h at room temperature. The reaction mixture was quenched with saturated aqueous NH4Cl at 0° C. and extracted with EtOAc. The combined organic layers were washed with H2O, then with saturated aqueous NaCl, and dried (MgSO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography (silica gel) using n-hexane:acetone (2:1→1:1, v/v) to afford 0.017 g of 2a (18% yield) and 0.030 g of 10 (27% yield), m.p. 170°-172° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05861388
출처 데이터셋uspto-grants-1999_01
ORD IDord-3cf41a3f2a0c453982aa15a49fad71b4
출처 메모uspto-grants-1999_01