HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451393Generated: October 31, 2026
Ammonia → 4-Thiazolemethanol, alpha-(bromomethyl)-2-(trifluoromethyl)-
https://huagongshe.com/reaction/1451393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10978660 | HCID 10978660 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Thiazolemethanol, alpha-(bromomethyl)-2-(trifluoromethyl)- | HCID 22220499 | — |
Reaction Steps
6 g (0.022 mol) of 2-Trifluoromethyl-4-bromoacetyl-thiazole are dissolved in 150 ml of methanol, and the solution is cooled to 10° C. and 0.63 g of sodium borohydride is added. After 15 minutes ice is added, and the mixture is acidified with hydrochloric acid, made alkaline with ammonia and extracted by shaking with methylene chloride. The organic phase is dried over sodium sulphate, filtered and concentrated. An oil is obtained and is reacted further as the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604225 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-da46e8d8a42d419fa1ec06949cf3316d |
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| Source note | uspto-grants-1997_02 |
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