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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647091Generated: November 1, 2026

Triethylamine → HCID 53979190, compound

https://huagongshe.com/reaction/1647091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBoc-L-ValineHCID 83693—
ReactantHCID 13089232HCID 13089232—
SolventDichloromethaneHCID 6344—
ProductHCID 53979190HCID 5397919024%

Reaction Steps

To a solution of N-(tert-butoxycarbony1)-L-valine (4.35 g) and triethylamine (2.13 g) in dry CH2Cl2 (40 ml) was added isobutyl chloroformate (2.87 g) at -20° C. After being stirred at same temperature for 30 minutes, a solution of N-(2-indanyl)glycine benzyl ester (5.37 g) in dry CH2Cl2 (20 ml) was added at -20° C. The reaction mixture was stirred at -10° C. for one hour then at room temperature for 4 hours. After the reaction mixture was evaporated under reduced pressure, the residue was dissolved in ethyl acetate (100 ml) and washed with saturated aqueous sodium bicarbonate (100 ml×2). The organic layer was dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified with silica gel (50 g) column chromatography (CHCl3:AcOEt=10:1) to give N-(tert-butoxycarbonyl)-L-valyl-N-(2-indanyl)glycine benzyl ester (2.20 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05430025
Source datasetuspto-grants-1995_07
ORD IDord-4e182b9e1d8c4c478f3845c803327ecd
Source noteuspto-grants-1995_07