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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium sulfite pentahydrate | HCID 19790054 | — |
| Reactant | tert-Butyl N-(1,3-thiazol-2-ylmethyl)carbamate | HCID 23088785 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524951B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-7fac31958e3545f88e31ffa20cbf8b1d |
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| Source note | uspto-grants-2009_04 |
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