HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352721Generated: October 29, 2026
Water → Ethyl 2-(2-t-pentyloxycarbonylamino-1,3-thiazol-4-yl)acetate
https://huagongshe.com/reaction/2352721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Thiazoleacetic acid, 2-amino-, ethyl ester | HCID 104454 | — |
| Reactant | Carbonochloridic acid, 1,1-dimethylpropyl ester | HCID 15051328 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(2-t-pentyloxycarbonylamino-1,3-thiazol-4-yl)acetate | HCID 19978738 | — |
Reaction Steps
To a solution of ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate (14 g.) in a mixture of pyridine (40 g.) and methylene chloride (300 ml.) was gradually added diethyl ether solution of t-pentyl chloroformate (70 ml.) containing 0.35 mole of t-pentyl chloroformate over 10 minutes at -20° C. with stirring, and the mixture was stirred for 2 hours at the same temperature and further stirred for 0.5 hour at 0° C. After the reaction, the reaction mixture was poured into water (200 ml.), and then the organic layer was separated. The organic layer was washed with 2N hydrochloric acid, water, 5% sodium bicarbonate aqueous solution and water in turn and then dried over magnesium sulfate. The solvent was distilled off from the organic layer to give dark brown oil of ethyl 2-(2-t-pentyloxycarbonylamino-1,3-thiazol-4-yl)acetate (12 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04877873 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-d5e0c0b915fc4ba6b8a05c1247d9c8d3 |
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| Source note | uspto-grants-1989_10 |
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