HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34669Generated: October 29, 2026
Bromoacetic Acid → HCID 21298333, compound
https://huagongshe.com/reaction/34669
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | HCID 178471202 | HCID 178471202 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21298333 | HCID 21298333 | 152.7% |
Reaction Steps
2 g (8.6 mmol) of ethyl 3-(2-mercapto-4-methyl-1,3-thiazol-5-yl)propionate were initially introduced into 40 ml of dry DMF, and 1.49 g (8.6 mmol) of bromoacetic acid were added. After 2 hours, the solvent was removed in vacuo, and 3.8 g of ethyl 3-[2-(carboxymethylthio)-4-methyl-1,3-thiazol-5-yl]propionate were obtained as an oil. The crude product was taken up in 25 ml of ethanol, 33 ml of 1N sodium hydroxide solution were added, and the reaction mixture was heated at 50° C. After the reaction was complete, the ethanol was removed in vacuo, and the aqueous residue was taken up in concentrated hydrochloric acid at pH 3.0, and the solution was extracted with ethyl acetate. 1.6 g (71%) of the title compound were obtained from the organic phase after drying with MgSO4, evaporation and crystallization with diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762848 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-0a6ab1a84a264ed78f207559ac610c6f |
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| Source note | uspto-grants-1988_08 |
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