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HRID 453207생성일: 2026년 10월 23일

Hexachloroethane → Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-4-chloro-1H-indol-5-yl ester

https://huagongshe.com/ko/reaction/453207

반응식

참여 물질

역할이름HCID투입량
반응물HexachloroethaneHCID 6214—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물Ammonium ChlorideHCID 25517—
반응물Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl esterHCID 9975323—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
생성물Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-4-chloro-1H-indol-5-yl esterHCID 9977109—

반응 조건

온도-78 °C

반응 단계

Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl ester (9.26 g, 26.7 mmol) is dissolved in THF (250 mL), flushed with nitrogen and cooled to −78° C. TMEDA (5 mL, 33.1 mmol) is then added followed by sec-butyllithium (24.8 mL, 34.7 mmol) and the reaction is stirred for 30 minutes. Hexachloroethane (12.73 g, 53.8 mmol) in 50 mL of THF is added over 10 minutes to the reaction. The reaction is allowed to warm to room temperature overnight (15 hours). The reaction is cooled using an ice bath and a saturated ammonium chloride (aq) solution is added (150 mL). The mixture is then extracted with ethyl acetate, dried (sodium sulfate) and concentrated to obtain the title compound as an oil that is used without further purification. MS (ESI) m/z 381.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492393B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-26a414fae1374652bc482e624cbc5097
출처 메모uspto-grants-2013_07