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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894452Generated: October 30, 2026

Sodium borohydride → HCID 12953363, compound

https://huagongshe.com/reaction/894452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13041832HCID 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 numberUS04284426
Source datasetuspto-grants-1981_08
ORD IDord-893c725af0524902b0656f0cdec7ba90
Source noteuspto-grants-1981_08