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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453207Generated: October 25, 2026

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

https://huagongshe.com/reaction/453207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl esterHCID 9975323—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-4-chloro-1H-indol-5-yl esterHCID 9977109—

Reaction Conditions

Temperature-78 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492393B2
Source datasetuspto-grants-2013_07
ORD IDord-26a414fae1374652bc482e624cbc5097
Source noteuspto-grants-2013_07