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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384304Generated: November 1, 2026

Sodium borohydride → HCID 53640764, compound

https://huagongshe.com/reaction/1384304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21186660HCID 21186660—
SolventEthanolHCID 702—
ProductHCID 53640764HCID 5364076431.3%

Reaction Steps

A mixture of sodium borohydride (0.090 g, 2.38 mmol) and ethanol (5 mL) was stirred 10 min and then 1-(3,5-dimethyl-4-triisopropylsilyloxyphenyl)-2-(4-(4-trifluoromethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-one (1.30 g, 2.25 mmol in 25 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 0.408 g (31%) of (1R*,2R*)-1-(3,5-dimethyl-4-triisopropylsilyloxyphenyl)-2-(4-(4-trifluoromethylphenyl)-4-hydroxypiperidin-1-yl)-propan-1-ol which was suitable for use without further purification and had: mp 177-177.5° C. Analysis calculated for C32H48F3NO3Si.0.25 H2O: C, 65.78; H, 8.37; N, 2.40. Found: C, 65.65; H, 8.51; N, 2.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258827B1
Source datasetuspto-grants-2001_07
ORD IDord-2c1ce455dda348e19f70c4457dd65763
Source noteuspto-grants-2001_07