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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485121Generated: October 31, 2026

Benzyloxycarbonylglycine → HCID 85923149, compound

https://huagongshe.com/reaction/1485121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxycarbonylglycineHCID 14349—
Reactant2-(Trimethylsilyl)ethanolHCID 18013—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChloroformHCID 6212—
ProductHCID 85923149HCID 85923149—

Reaction Steps

To a mixture of N-[(benzyloxy)carbonyl]glycine (5.33 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.86 g), 1-hydroxybenzotriazole monohydrate (4.68 g) and chloroform (51.0 mL), 2-(trimethylsilyl)ethanol (4.36 mL) was added and the mixture was stirred at room temperature for 8 hours. To the reaction mixture, 2-(trimethylsilyl)ethanol (3.00 mL), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.93 g) and 4-dimethylaminopyridine (312 mg) were added and the mixture was stirred at room temperature for 65 hours. After pouring the reaction mixture into a saturated aqueous solution of ammonium chloride, three extractions were conducted with ethyl acetate. The combined organic layers were washed with saturated brine and dried over anhydrous magnesium sulfate. After removing the desiccant by filtration, the filtrate was concentrated under reduced pressure and purified by silica gel column chromatography (n-hexane:ethyl acetate=95:5-80:20) to give 2-(trimethylsilyl)ethyl N-[(benzyloxy)carbonyl]glycinate as a colorless oil (6.64 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-616297b7674345a58bfa9d9dda879dc0
Source noteuspto-grants-2016_08