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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080873Generated: October 26, 2026

Water → alpha-t-Butyloxycarbonylamino-alpha-[2-(chloroacetamido)thiazol-4-yl]acetic acid ethyl ester

https://huagongshe.com/reaction/1080873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroacetyl chlorideHCID 6577—
Reactantalpha-t-Butyloxycarbonylamino-alpha-(2-aminothiazol-4-yl)acetic acid ethyl esterHCID 12763199—
SolventDimethylacetamideHCID 31374—
Productalpha-t-Butyloxycarbonylamino-alpha-[2-(chloroacetamido)thiazol-4-yl]acetic acid ethyl esterHCID 1276320290.8%

Reaction Steps

To a solution of 1.26 g of α-t-butyloxycarbonylamino-α-(2-aminothiazol-4-yl)acetic acid ethyl ester in 5 ml of N,N-dimethylacetamide is added 708 mg of chloroacetyl chloride under stirring. After the stirring for further 1 hour at room temperature, the reaction solution is poured into water and extracted with ethyl acetate. The organic layer is washed with saturated sodium bicarbonate aq. solution and then water and dried over anhydrous magnesium sulfate. The distillation of the solvent gives 1.435 g of α-t-butyloxycarbonylamino-α-[2-(chloroacetamido)thiazol-4-yl]acetic acid ethyl ester as crystals (yield, 90.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583216
Source datasetuspto-grants-1996_12
ORD IDord-4a41412eab644cb8b7d3da470457fdae
Source noteuspto-grants-1996_12