Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128815Generated: October 25, 2026

Water → 2-(Octylthio)thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/128815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromooctaneHCID 8140—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178470113HCID 178470113—
SolventDimethylformamideHCID 6228—
Product2-(Octylthio)thiazole-4-carboxylic acid ethyl esterHCID 5452686578%

Reaction Steps

To a solution of 2-mercaptothiazole-4-carboxylic acid ethyl ester (Zhelyazkov, L.; Todorova, N.; Manolova, P. Tr. Nauchnoizsled. Khim.-Farm. Inst., 9, 59-67 (1974); Chem. Abstr., 83, 58706 q) (3.0 g) in DMF (20 ml) is added sodium hydride (0.70 g of 60% dispersion). After 10 min, 1-bromooctane (3.0 ml) is added, and the mixture is stirred at 60° for 30 min. The mixture is poured into water and extracted with ether, and the extracts are dried, filtered, and concentrated. The residue is recrystallized from hexane to provide 2-(octylthio)thiazole-4-carboxylic acid ethyl ester as a colorless solid (3.7 g, 78%). This material is reduced in the usual fashion with lithium aluminum hydride in THF, providing 2-(octylthio)thiazole-4-methanol (2.12 g, 67%) as a colorless oil after chromatography. This is combined with DDQ (1.8 g) in 1,4-dioxane (25 ml) and stirred for 48 hr at room temperature. The reaction mixture is filtered, and the filtrate is concentrated and chromatographed with dichloromethane to provide 2-(octylthio)thiazole-4-carboxaldehyde as a tan solid (1.67 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464865
Source datasetuspto-grants-1995_11
ORD IDord-98e1c24e5a604cc69a49499f9b1264e5
Source noteuspto-grants-1995_11