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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230031Generated: October 23, 2026

Sodium Hydroxide → 5-Bromo-2-formylaminomethylthiazole

https://huagongshe.com/en/reaction/230031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BromideHCID 253881—
ReactantFormamide, N-(2-thiazolylmethyl)-HCID 22916723—
ReactantSodium Phosphate, Monobasic, DihydrateHCID 23673460—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-formylaminomethylthiazoleHCID 2308876233.6%

Reaction Conditions

Temperature30 °C

Reaction Steps

2-Formylaminomethylthiazole (200 g) was added to a solution of 4.5 kg of sodium dihydrogenphosphate dihydrate in 6 L of water, and the mixture was stirred at 30° C. Sodium bromide (4.0 kg) and 2 L of tetrahydrofuran were added thereto in that order. Bromine (1.49 kg) was added while adjusting the solution to pH 3 by the addition of a 6 N aqueous sodium hydroxide solution, and the mixture was stirred for 2 hr. The reaction mixture was added to a solution of 500 g of sodium sulfite in 4 L of water to stop the reaction and was then adjusted to pH 4.9 by the addition of a 6 N aqueous sodium hydroxide solution while maintaining the temperature of the mixture at 30° C. The reaction mixture was extracted with 10 L of ethyl acetate and then with 5 L of ethyl acetate. The organic layers were combined and were dried over anhydrous magnesium sulfate. The solvent was removed to bring the volume to 1 L, and the concentrate was stirred at 6° C. for 12 hr for crystallization to give 104.4 g of 5-bromo-2-formylaminomethylthiazole. The results of NMR analysis were in agreement with the results of analysis in Example 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563901B2
Source datasetuspto-grants-2009_07
ORD IDord-38e4c5a8df834501bcd5cf4e974baea1
Source noteuspto-grants-2009_07