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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669270Generated: October 30, 2026

Sodium borohydride → HCID 67342731, compound

https://huagongshe.com/reaction/1669270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67342066HCID 67342066—
SolventEthanolHCID 702—
ProductHCID 67342731HCID 67342731—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-[2-(4-Trifluoromethyl-phenyl)-pyrimidin-5-yl]-heptan-1-one (1.47 g, 4.36 mmol) is dissolved in ethanol and cooled to 0° C. while stirring under nitrogen. To the flask is added sodium borohydride (165 mg, 4.36 mmol), and the reaction is kept at 0° C. for 1 h., then slowly warmed to room temperature. The reaction is monitored by HPLC. Upon complete consumption of starting material, the reaction is carefully quenched with water, the ethanol removed by rotary evaporator, and extracted with diethyl ether, washed, dried, and concentrated. The title compound is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989457B2
Source datasetuspto-grants-2011_08
ORD IDord-140af3cfd7d54359a338f149a0d8ac03
Source noteuspto-grants-2011_08