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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985421Generated: October 30, 2026

Triethylamine → HCID 22927019, compound

https://huagongshe.com/reaction/1985421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 22926821HCID 22926821—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22927019HCID 2292701949.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.3 g of Ethyl 3-(1-carboxymethyl-1H-indol-3-yl)-2-isopropoxypropionate was dissolved in 10 ml of tetrahydrofuran, and 0.2 ml of triethylamine was added under ice-cooling, followed by 0.1 ml of ethyl chloroformate, then the mixture was stirred at 0° C. for 15 minutes. After filtering off the precipitated insoluble substances, the reaction solution was again cooled with ice, and 60 mg of sodium borohydride and water were added, and stirring was continued at room temperature for 1 hour. The reaction solution was cooled with ice, acidified with diluted hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and evaporated. The residue was subjected to silica gel column chromatography (33% ethyl acetate-hexane), to give 143 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544835B2
Source datasetuspto-grants-2009_06
ORD IDord-da069425df1e4fd79d8e85a6a5d10e95
Source noteuspto-grants-2009_06