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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465293Generated: October 26, 2026

Tetrahydrofuran → N-(cholest-5-ene-3beta-oxycarbonyl)glycylglycine

https://huagongshe.com/reaction/465293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantGlycylglycineHCID 11163—
ReactantSodium BicarbonateHCID 516892—
ReactantC28H45ClO2HCID 54236888—
SolventWaterHCID 962—
ProductN-(cholest-5-ene-3beta-oxycarbonyl)glycylglycineHCID 13171755280.8%

Reaction Steps

Sodium hydrogencarbonate (0.168 g) and tetrahydrofuran (20 ml) were added to a suspension of glycylglycine (0.15 g) in water (20 ml). After tetrahydrofuran (20 ml) and cholesteryl chloroformate (0.898 g) were added to the resulting transparent solution at 0° C., the mixture was stirred for an hour. The reaction mixture was concentrated under reduced pressure and, methanl (10 ml) and chloroform (10 ml) were added to the residue. By filtration, the transparent solution was obtained. The solvent was distilled off to give crude crystals (0.98 g). The crude crystals were then purified by silica gel chromatography to give N-(cholest-5-ene-3β-oxycarbonyl)glycylglycine (0.5 g) as white powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05152999
Source datasetuspto-grants-1992_10
ORD IDord-c01942f2ad344ee7b3deac1007c75775
Source noteuspto-grants-1992_10