HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638424Generated: October 25, 2026
Sodium borohydride → Ethyl 2-hydroxy-2-(2-mesylamino-1,3-thiazol-4-yl)acetate
https://huagongshe.com/reaction/638424
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 2-(2-mesylamino-1,3-thiazol-4-yl)glyoxylate | HCID 19978726 | — |
| Reactant | HCID 178473045 | HCID 178473045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-hydroxy-2-(2-mesylamino-1,3-thiazol-4-yl)acetate | HCID 20254378 | — |
Reaction Steps
To a mixture of ethyl 2-(2-mesylamino-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-mesylimino-2,3-dihydro-1,3-thiazol-4-yl)glyoxylate, (3.60 g.) and ethanol (50 ml.) was added sodium borohydride (0.32 g.) under stirring and ice-cooling, and then the mixture was stirred for 40 minutes at room temperature. After the reaction, the reaction mixture was concentrated. The residue was poured into a mixture of ethyl acetate (100 ml.) and dilute hydrochloric acid, and the aqueous solution was separated. Thus obtained aqueous solution (pH 1 to 2) was subjected to salting-out and then extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The extract was treated with activated charcoal and then the solvent was distilled off to give a solid of ethyl 2-hydroxy-2-(2-mesylamino-1,3-thiazol-4-yl)acetate, which can be represented as ethyl 2-hydroxy-2-(2-mesylimino-2,3-dihydro-1,3-thiazol-4-yl)acetate, (2.6 g.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560765 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-9c7fdc1e98d147ff8787c15b6c61c3ce |
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| Source note | uspto-grants-1985_12 |
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