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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647090Generated: October 25, 2026

Tetrahydrofuran → HCID 70050348, compound

https://huagongshe.com/reaction/1647090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantDiphosgeneHCID 10426—
ReactantMethyl 4-aminobenzoateHCID 12082—
Reactantbenzyl (2S)-2-amino-3-methylbutanoateHCID 6950584—
ProductHCID 70050348HCID 70050348—

Reaction Steps

To a solution of methyl p-aminobenzoate (0.4 g) in tetrahydrofuran (10 ml) was added trichloromethylchloroformate (0.31 g) and the mixture was allowed to stand overnight at room temperature. L-Valine benzyl ester (0.54 g) was added to the solution and the pH of the mixture was neutralized with triethylamine. After being stirred for 30 minutes at room temperature, the mixture was concentrated under reduced pressure and the residue was extracted with ethyl acetate (10 ml). The extract was washed with 1N-hydrochloric acid (10 ml) and aqueous sodium bicarbonate (10 ml) and concentrated to dryness to give 4-(methoxycarbonyl)phenylaminocarbonyl-L-valine benzyl ester (1.17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05430025
Source datasetuspto-grants-1995_07
ORD IDord-1760c07e0d5546cf8f11bd102b954cdf
Source noteuspto-grants-1995_07