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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 2-(2-mesylamino-1,3-thiazol-4-yl)glyoxylateHCID 19978726—
ReactantHCID 178473045HCID 178473045—
SolventEthanolHCID 702—
ProductEthyl 2-hydroxy-2-(2-mesylamino-1,3-thiazol-4-yl)acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560765
Source datasetuspto-grants-1985_12
ORD IDord-9c7fdc1e98d147ff8787c15b6c61c3ce
Source noteuspto-grants-1985_12