HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050710Generated: October 26, 2026
Ethylamine → N-((2-Chlorothiazol-5-yl)methyl)ethanamine
https://huagongshe.com/reaction/1050710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-5-chloromethylthiazole | HCID 2763179 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-((2-Chlorothiazol-5-yl)methyl)ethanamine | HCID 22450338 | — |
Reaction Steps
A 60˜70% aqueous solution of ethylamine (3.6 mL) and a 20% aqueous NaOH solution (8.0 mL) were added dropwise respectively into a solution of 2-chloro-5-chloromethylthiazole (3.40 g) in chloroform (40 mL), then benzyl triethyl ammonium chloride (0.1 g) was added. After stirring overnight at room temperature, the pH of the resulting mixture was adjusted to weak alkaline. The organic layer was separated while the aqueous layer was extracted with dichloromethane twice. The organic phases were combined, and dried over anhydrous sodium sulfate after washed with an iced aqueous sodium chloride solution twice, then remove the solvent under reduced pressure to obtain 2-chloro-5-ethylaminomethylthiazole 3.37 g as an oil in 95.2% purity. GC-MS: (M+) (EI, 70 eV, m/z) calc: 176. found: 176.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09386769B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-c9d488a28e0f477f8546e96f6b97a188 |
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| Source note | uspto-grants-2016_07 |
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