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HRID 450293作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/450293

反応式

関与物質

役割名称HCID仕込み量
反応物HexachloroethaneHCID 6214—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物Ammonium ChlorideHCID 25517—
反応物Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl esterHCID 9975323—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
生成物Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-4-chloro-1H-indol-5-yl esterHCID 9977109—

反応条件

温度-78 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08486954B2
出典データセットuspto-grants-2013_07
ORD IDord-ed2e015faf7148bebe191541f8f80ee1
出典メモuspto-grants-2013_07