HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32817Generated: October 30, 2026
Trifluoroacetic acid → 1-(2-Amino-1,3-thiazol-4-yl)propan-1-one
https://huagongshe.com/reaction/32817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl (4-propionylthiazol-2-yl)carbamate | HCID 45117897 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Amino-1,3-thiazol-4-yl)propan-1-one | HCID 45121692 | 75.5% |
Reaction Steps
(4-Propionyl-thiazol-2-yl)-carbamic acid tert-butyl ester (5.0 g, 19.5 mmol) was suspended in dichloromethane (100 mL) at 0° C. Trifluoroacetic acid (100 mL) was added and the mixture was stirred at 0° C. for 1.5 hours. The cooling bath was removed and stirring was continued for 1 hour prior to concentration of the reaction mixture in vacuo. The residue was triturated with ether and filtered. The solid was dissolved in a mixture of dichloromethane and saturated aqueous sodium bicarbonate solution. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic extracts were washed with brine, dried over sodium sulfate and evaporated to give 1-(2-amino-thiazol-4-yl)-propan-1-one (2.3 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07427635B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-131e9f6cf7aa489aaba0f33c4226b354 |
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| Source note | uspto-grants-2008_09 |
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