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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003610Generated: November 1, 2026

Sodium borohydride → HCID 54480353, compound

https://huagongshe.com/reaction/1003610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21186659HCID 21186659—
SolventEthanolHCID 702—
ProductHCID 54480353HCID 5448035365%

Reaction Steps

A mixture of sodium borohydride (0.085 g, 2.25 mmol) and ethanol (5 mL) was stirred 10 min and then 1-(4-benzyloxy-3,5-difluorophenyl)-2-(4-(4-trifluoromethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-one (1.02 g, 1.96 mmol in 30 mL of ethanol) was added. The reaction was stirred at ambient temperature overnight. The white solid which precipitated was collected by filtration and dried to yield 0.66 g (65%) of (1R*,2R*)-1-(4-benzyloxy-3,5-difluorophenyl)-2-(4-(4-trifluormethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-ol which was suitable for use without further purification and had: mp 201-202° C. Analysis calculated for C28H28F5NO3.0.25 H2O: C, 63.93; H, 5.46; N, 2.66. Found: C, 63.98; H, 5.49; N, 2.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046213
Source datasetuspto-grants-2000_04
ORD IDord-374cc261f0f145ff96cbd81786fb7a3d
Source noteuspto-grants-2000_04