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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 343302생성일: 2026년 10월 24일

Hydrochloric Acid → 2-Formyl-17beta-estradiol

https://huagongshe.com/ko/reaction/343302

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물HexamethylenetetramineHCID 4101—
반응물EstradiolHCID 5757—
반응물Trifluoroacetic acidHCID 6422—
반응물Potassium CarbonateHCID 11430—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-Formyl-17beta-estradiolHCID 999498013%
생성물4-Formyl-17beta-estradiolHCID 117223424%

반응 조건

온도100 °C

반응 단계

To a mixture of estradiol (1, 13.6 g, 50 mmol) and hexamethylenetetramine (21.0 g, 150 mmol) was added trifluoroacetic acid (100 mL) at room temperature. The reaction mixture was stirred for 6 h at 100° C., poured into H2O (300 mL), and extracted with Et2O. 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 dissolved in THF (50 mL) and MeOH (50 mL), potassium carbonate (6.9 g, 50 mmol) was added, and the mixture stirred for 1 h at room temperature. The reaction mixture was then diluted with EtOAc, acidified with 1N HCl, 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:THF (5:1→3:1, v/v) to afford 1.91 g of 2a (13% yield), m.p. 219°-221° C., and 0.552 g of 2b (4% yield), m.p. 146°-147° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05861388
출처 데이터셋uspto-grants-1999_01
ORD IDord-64e0a4d0429e46eca901b4385d431ffc
출처 메모uspto-grants-1999_01