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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255071Generated: October 31, 2026

Hydrogen Bromide → 2-Bromo-1-(2-methyl-thiazol-5-yl)-ethanone

https://huagongshe.com/reaction/1255071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant2-Methyl-1,3-thiazole-4-carbonyl chlorideHCID 21183959—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-Bromo-1-(2-methyl-thiazol-5-yl)-ethanoneHCID 2166758287%

Reaction Steps

To a solution of 2-methylthiazole-4-carbonyl chloride (0.34 g, 2.10 mmol) in dry MeCN (8 mL) cooled at 0° C., under nitrogen atmosphere, is slowly added (diazomethyl)trimethylsilane (3.14 ml, 6.29 mmol, 2.0M in hexane). The reaction is stirred at RT for 15 h (UPLC-MS monitoring: complete conversion). The reaction is cooled at 0° C. and 48% hydrobromic acid (1.23 mL, 7.34 mmol) is added dropwise. The reaction is stirred at RT for 3 hour. Then EtOAc and water are added, the organic layer is separated and the aqueous phase is neutralized with 1M NaOH and extracted with EtOAc. The combined organic layers are dried over Na2SO4, filtered and evaporated to dryness to obtain compound I228 as a dark brown gummy solid (400 mg, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455646B2
Source datasetuspto-grants-2013_06
ORD IDord-57581344565f4807beb756c3f09935ca
Source noteuspto-grants-2013_06