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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 343307생성일: 2026년 10월 24일

Hydrochloric Acid → 3-Hydroxy-17-methyleneestra-1,3,5(10)-triene-2-carboxaldehyde

https://huagongshe.com/ko/reaction/343307

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Ethyl BromideHCID 6332—
반응물HexamethylphosphoramideHCID 12679—
반응물MagnesiumHCID 5462224—
반응물17-Methylene-estra-1,3,5(10)-trien-3-olHCID 14458552—
용매BenzeneHCID 241—
용매TetrahydrofuranHCID 8028—
생성물3-Hydroxy-17-methyleneestra-1,3,5(10)-triene-2-carboxaldehydeHCID 5427244978.2%

반응 단계

To a suspension of magnesium (0.365 g, 15 mmol) in THF (3.0 mL) was added bromoethane (1.5 mL, 20 mmol) dissolved in THF (3.0 mL) at room temperature. 17-Methyleneestra-1,3,5(10)-trien-3-ol (19, 0.805 g, 3.0 mmol) dissolved in THF (7.5 mL) was added to the reaction mixture, and stirring continued for 30 min. The solvent was removed at reduced pressure, and to the residue were added benzene (35 mL), hexamethylphosphoric triamide (1.4 mL, 7.5 mmol) and paraformaldehyde (0.630 g). Stirring was continued for 6 h at 80° C. After the reaction mixture was cooled to room temperature, 5N HCl (15 mL) was added and the mixture extracted with EtOAc. The combined organic layers were washed with H2O, then with saturated aqueous NaCl, and dried (Na2SO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography (silica gel) using n-hexane:AcOEt (10:1→3:1, v/v) to afford 0.695 g of 23 (78% yield), m.p. 128°-130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05861388
출처 데이터셋uspto-grants-1999_01
ORD IDord-e7eaae67874d4c4495113894041f5713
출처 메모uspto-grants-1999_01