HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127103Generated: October 25, 2026
Ethyl Acetate → 2-(2-Methanesulfonamido-1,3-thiazol-4-yl)acetic acid
https://huagongshe.com/reaction/127103
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-methanesulfonamidothiazol-4-ylacetate | HCID 3145078 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Methanesulfonamido-1,3-thiazol-4-yl)acetic acid | HCID 3159575 | 73% |
Reaction Steps
To a solution of potassium hydroxide (2.9 g.) in water (80 ml.) was added ethyl 2-methanesulfonamidothiazol-4-ylacetate (9.1 g.) under ice-cooling and stirring, and the mixture was stirred for 1 hour at room temperature. After the reaction, to the reaction mixture was added a mixture of water and ethyl acetate, and then the aqueous layer was separated. The remaining ethyl acetate layer was extracted twice with 10% hydroxide aqueous solution. The extracts were combined with the above obtained aqueous layer, and the mixture was acidified with hydrochloric acid under ice-cooling. The precipitated crystals were collected by filtration, washed with water and dried to give 2-methanesulfonamidothiazol-4-ylacetic acid (5.94 g.), mp 158°-160° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254260 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-b087c7777af54fa09f7e39a51b4c0f64 |
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| Source note | uspto-grants-1981_03 |
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