HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65519Generated: October 27, 2026
Ethyl Acetate → 2-(2-aminothiazol-4-yl)thioacetic acid-S-ethyl ester
https://huagongshe.com/reaction/65519
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 4-bromo-3-oxothiobutyric acid-S-ethyl ester | HCID 13821657 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-(2-aminothiazol-4-yl)thioacetic acid-S-ethyl ester | HCID 13821654 | 65.5% |
Reaction Steps
In 7.0 ml of N,N-dimethylacetamide was dissolved 2.25 g of the 4-bromo-3-oxothiobutyric acid-S-ethyl ester obtained in Referential Example 4-(1), and 1.14 g of thiourea was added to the resulting solution with ice-cooling, after which the resulting mixture was subjected to reaction at room temperature for 1 hour. The reaction mixture was introduced into a mixed solvent of 50 ml of ethyl acetate and 50 ml of water, and the pH was adjusted to 6.0 with sodium hydrogencarbonate. Then, the organic layer was separated, washed with two 50-ml portions of water and with 50 ml of saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. Then the solvent was removed by distillation under reduced pressure. The residue obtained was recrystallized from 20 ml of ethyl acetate to obtain 1.32 g (yield, 65.5%) of 2-(2-aminothiazol-4-yl)thioacetic acid-S-ethyl ester having a melting point of 76°-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04614819 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-5b30943ef83441d39a27c23d957e3439 |
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| Source note | uspto-grants-1986_09 |
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