Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415010Generated: October 28, 2026

Triethylamine → 2-Azidomethyl-4-bromo-thiazole

https://huagongshe.com/reaction/415010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium AzideHCID 33557—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
Reactant(4-Bromo-1,3-thiazol-2-yl)methanolHCID 11041630—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Azidomethyl-4-bromo-thiazoleHCID 57985611—

Reaction Steps

(4-Bromo-thiazol-2-yl)-methanol (1.1 g, 5.7 mmol) in DMF (15 ml) is treated at room temperature under nitrogen atmosphere with trifluoromethanesulfonyl chloride (0.61 ml, 1 equivalent), and Et3N (0.8 ml, 1 equivalent). The reaction mixture is stirred for 3 hours at room temperature before the addition of sodium azide (1.11 g, 3 equivalents), followed by overnight stirring at the same temperature. The reaction mixture is diluted with water and extracted with DCM and diethyl ether. The combined organic extracts are dried (MgSO4) and concentrated under reduced pressure to afford the crude product, which is used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088766B2
Source datasetuspto-grants-2012_01
ORD IDord-8a323b20ed364551a6b9fa1a96b21976
Source noteuspto-grants-2012_01