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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387253Generated: October 30, 2026

Triethylsilane → HCID 59332568, compound

https://huagongshe.com/reaction/387253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantDihydro-3(2H)-thiophenoneHCID 61252—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 5-bromo-1H-indole-7-carboxylateHCID 59332585—
SolventDichloromethaneHCID 6344—
ProductHCID 59332568HCID 5933256846.5%

Reaction Steps

To the stirred mixture of dihydro-3(2H)-thiophenone (0.167 mL, 1.97 mmol) in DCM (25 mL) under N2 was added TMS-OTf (0.71 mL, 3.9 mmol) slowly over about 5 minutes at 0° C. (ice-bath). A solution of ethyl 5-bromo-1H-indole-7-carboxylate (0.50 g, 1.97 mmol) in DCM (5 mL) was added dropwise over 60 min, then triethylsilane (1.26 mL, 9.8 mmol) was added in one portion, and the reaction was allowed to warm slowly to room temperature. Then saturated NaHCO3 and DCM were added, the layers were separated and the aqueous layer was extracted with DCM twice. The combined organic layers were dried (MgSO4) and concentrated. The residue was purified using Companion, giving 312 mg (46%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372875B2
Source datasetuspto-grants-2013_02
ORD IDord-89429d394183426489fa554e03d1d727
Source noteuspto-grants-2013_02