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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387262Generated: October 25, 2026

Triethylsilane → methyl 5-bromo-3-(4-thiepanyl)-1H-indole-7-carboxylate

https://huagongshe.com/reaction/387262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantThiepan-4-oneHCID 15698157—
Reactantmethyl 5-bromo-1H-indole-7-carboxylateHCID 24728848—
SolventDichloromethaneHCID 6344—
Productmethyl 5-bromo-3-(4-thiepanyl)-1H-indole-7-carboxylateHCID 5933270634.3%

Reaction Steps

To a flask under argon in an ice-bath, the 4-thiepanone (200 mg, 1.536 mmol) in 6 mL of dried CH2Cl2 was first dried w/4 A sieves and then transferred via a double needle tubing (cannula). TMS-OTf (278 uL, 1.536 mmol) was added dropwise and the reaction was stirred for 10 min. A solution of methyl 5-bromo-1H-indole-7-carboxylate (390 mg, 1.536 mmol) in 7 mL of CH2Cl2 was dried with 4 A sieves and then added into above solution dropwise. Stirring continued for 4 hours and the reaction was warmed to room temperature. The mixture was cooled to 0° C. and triethylsilane (245 uL, 1.536 mmol) was added as one portion. The mixture was stirred overnight then warmed to room temperature. The mixture was quenched water and sat. NaHCO3, then diluted water/AcOEt and washed with H2O and brine. 194 mg of crude product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372875B2
Source datasetuspto-grants-2013_02
ORD IDord-66a71348ceb742b7a75b84aee0a3e8f2
Source noteuspto-grants-2013_02