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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460024Generated: October 30, 2026

Sodium borohydride → HCID 86592484, compound

https://huagongshe.com/reaction/460024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58824789HCID 58824789—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86592484HCID 86592484—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of ethyl [2-methyl-4-(3-{4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}propanoyl)phenoxy]acetate (intermediate11, 0.28 g) in tetrahydrofuran (8 ml) and water (8 ml) at 0° C. was treated portion-wise with sodium borohydride (0.043 g) and the mixture was stirred at 0° C. for 1 hour. The solvent was evaporated and the residue partitioned between water and ethyl acetate; the aqueous layer was separated and extracted twice more with ethyl acetate. The combined organic solutions were dried with brine and over magnesium sulfate and concentrated. The product isolated after evaporation of the solvent was further purified by flash column chromatography using cyclohexane:ethyl acetate (3:1) as eluent to give the title compound as a colourless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196107B2
Source datasetuspto-grants-2007_03
ORD IDord-12d38a5839a548ea9d5d7c4b43366b39
Source noteuspto-grants-2007_03