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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 534273생성일: 2026년 10월 24일

Potassium Carbonate → Ethyl 2-(7-hydroxy-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetate

https://huagongshe.com/ko/reaction/534273

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Boron tribromideHCID 25134—
반응물Ethyl 2-(7-methoxy-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetateHCID 67211141—
용매DichloromethaneHCID 6344—
생성물Ethyl 2-(7-hydroxy-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetateHCID 5334567520.4%

반응 조건

온도-2.5 °C

반응 단계

DCM (305 mL) was transferred to a 1 L 3-necked round-bottomed flask and cooled to −11° C. (internal) (ice acetone bath). BBr3 (72.0 mL, 761 mmol) was added to the DCM with stirring. A solution of ethyl 2-(7-methoxy-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetate (41.62 g, 152 mmol) in DCM (145 mL) was added in drops maintaining the internal temperature of about −5 to 0° C. After the addition the reaction was stirred for 1 h below about 0° C. The reaction mixture was slowly poured into mixture of ice (400 mL) and saturated K2CO3 (400 mL) and stirred well (pH maintained at 9-7). The organic layer was separated, washed with brine (1×100 mL), dried over MgSO4, filtered and concentrated under reduced pressure. The residual brown oil was purified by passing it through a pad of silica gel to give the title compound (8.03 g). LCMS m/z=260.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853419B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-06dd1b295cc4421392069cee397982bf
출처 메모uspto-grants-2014_10