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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113283Generated: October 30, 2026

Bromine → Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate

https://huagongshe.com/reaction/2113283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
ReactantSodium sulfite pentahydrateHCID 19790054—
Reactanttert-Butyl N-(1,3-thiazol-2-ylmethyl)carbamateHCID 23088785—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl ((5-bromothiazol-2-yl)methyl)carbamateHCID 23088769—

Reaction Steps

A solution (2 L) of 1.33 kg of 2-t-butoxycarbonylaminomethylthiazole in ethyl acetate was added to an aqueous solution (20 L) of 8.6 kg of sodium acetate, and the mixture was stirred. Bromine (1.35 L) was added dropwise to this solution (internal temperature: 19 to 24° C.) over a period of 3.5 hr, and the mixture was stirred at an internal temperature of 25.5±5° C. for 14 hr. Sodium sulfite pentahydrate (180 g) was added thereto, the mixture was then extracted with 3 L of ethyl acetate, and the organic layer was washed with 1 L of water and 1.53 L of a 6 M aqueous sodium hydroxide solution. The aqueous layer was then extracted with 3 L of ethyl acetate. The organic layers were combined, were dried over anhydrous magnesium sulfate, and were filtered. The solvent was removed from the filtrate by evaporation under the reduced pressure, followed by substitution concentration twice with 2 L of ethanol to give 944 g of 5-bromo-2-t-butoxycarbonylaminomethylthiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524951B2
Source datasetuspto-grants-2009_04
ORD IDord-7fac31958e3545f88e31ffa20cbf8b1d
Source noteuspto-grants-2009_04