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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178470113 | HCID 178470113 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Octylthio)thiazole-4-carboxylic acid ethyl ester | HCID 54526865 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05464865 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-98e1c24e5a604cc69a49499f9b1264e5 |
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| Source note | uspto-grants-1995_11 |
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