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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223627Generated: November 1, 2026

alpha-t-Butyloxycarbonylamino-alpha-[2-(trichloroethoxycarbonylamino)thiazol-4-yl)acetic acid ethyl ester → alpha-t-Butyloxycarbonylamino-alpha-(2-aminothiazol-4-yl)acetic acid ethyl ester

https://huagongshe.com/reaction/223627

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-t-Butyloxycarbonylamino-alpha-[2-(trichloroethoxycarbonylamino)thiazol-4-yl)acetic acid ethyl esterHCID 12763205—
CatalystZincHCID 23994—
SolventFormic AcidHCID 284—
Productalpha-t-Butyloxycarbonylamino-alpha-(2-aminothiazol-4-yl)acetic acid ethyl esterHCID 1276319971.2%

Reaction Steps

To a solution of 2.80 g of α-t-butyloxycarbonylamino-α-[2-(trichloroethoxycarbonylamino)thiazol-4-yl]acetic acid ethyl ester in 60 ml of 90% formic acid is added 2.80 g of zinc dust under cooling and stirring. The mixture is stirred for 1 hour and zinc dust is filtered off. The filtrate is poured into water and the resultant solution is 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 1.26 g (yield, 71.2%) of α-t-butyloxycarbonylamino-α-(2-aminothiazol-4-yl)acetic acid ethyl ester as crystals. Melting point: 143°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355160
Source datasetuspto-grants-1982_10
ORD IDord-8be70d82d1ec42db8d509e07e4d2bfeb
Source noteuspto-grants-1982_10