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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859957Generated: October 26, 2026

Benzyl chloroformate → Ethyl-2-benzyloxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate

https://huagongshe.com/reaction/859957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantEthyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductEthyl-2-benzyloxycarbonyloxyamino-4-methyl-thiazole-5-carboxylateHCID 2191146748%

Reaction Steps

A 3 M aq. NaHCO3 solution (10 mL, 30 mmol) was added to a stirred solution of ethyl-2-amino-4-methyl-thiazole-5-carboxylate (372 mg, 2 mmol) in THF (20 mL) at 0–5° C. Benzyl chloroformate (500 μL) was added. After 2 h, additional benzyl chloroformate (500 μL) and the biphasic solution was stirred for an additional 2 h at 0–5° C. The mixture was diluted with dichloromethane (50 mL) and water (30 mL). The organic layer was separated, dried (MgSO4), filtered and concentrated. The residue was chromatographed on a silica gel column. Elution with 10% EtOAc in hexanes followed by 20% and 30% EtOAc in hexanes afforded the title compound (310 mg, 48%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153856B2
Source datasetuspto-grants-2006_12
ORD IDord-b67f3335218e4819af7db007784e7260
Source noteuspto-grants-2006_12