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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757911Generated: November 2, 2026

Sodium borohydride → HCID 12953363, compound

https://huagongshe.com/reaction/1757911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 2-chloro-4-(p-chlorophenyl)-5-thiazolecarboxylateHCID 13041832—
SolventEthanolHCID 702—
ProductHCID 12953363HCID 129533637%

Reaction Steps

To a suspension of 18.2 g (0.06 mol) of ethyl 2-chloro-4-(p-chlorophenyl)-5-thiazolecarboxylate in 100 ml of ethanol was added 2.27 g (0.06 mol) of sodium borohydride. The reaction mixture was stirred for 1 hour and filtered. The ethanol filtrate was concentrated under reduced pressure and the residue was treated with water and extracted with CHCl3. The CHCl3 extracts were dried over MgSO4 and concentrated under reduced pressure. The residual solid (1.5 g) was recrystallized from ethanol-water to give 1.1 g (6%) of 2-chloro-4-(p-chlorophenyl)-5-thiazolemethanol, mp 113°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371389
Source datasetuspto-grants-1983_02
ORD IDord-a9d907a960cb46c7844ac193bece6e21
Source noteuspto-grants-1983_02