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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492443Generated: November 2, 2026

Sodium bis(trimethylsilyl)amide → (E)-Ethyl 3-[2-(phenylcarbamoyl)ethenyl]-1-(2-trimethylsilylethoxymethyl)-4,6-dichloroindole-2-carboxylate

https://huagongshe.com/reaction/1492443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantHCID 10834984HCID 10834984—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(E)-Ethyl 3-[2-(phenylcarbamoyl)ethenyl]-1-(2-trimethylsilylethoxymethyl)-4,6-dichloroindole-2-carboxylateHCID 1895106978.4%

Reaction Steps

To a cooled (0°) solution of (E)-Ethyl-3-[2-(phenylcarbamoyl)ethenyl]-4,6-dichloroindole-2-carboxylate (300 mg) in dry DMF (25 ml) a solution of sodium bis-(trimethylsilyl)amide (1M;0.0814 ml) was added dropwise. The resulting mixture was stirred at room temperature for 30 minutes then cooled to 0°. Trimethylsilylethoxymethylchloride (185 mg) was added, and the reaction was stirred for one hour at room temperature. The resulting solution was poured in H2O (20 ml) and extracted with diethylether (15 ml×3). The organic layers were dried, concentrated under vacuum and the product isolated by chromatography on silica gel(CH/EA:83/15) to give the title compound (311 mg). Rf =0.35 CH/EA:85/15

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374648
Source datasetuspto-grants-1994_12
ORD IDord-e74a931767a64d3e9c32e7a61ee6aa0e
Source noteuspto-grants-1994_12