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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003609Generated: October 31, 2026

Sodium borohydride → HCID 53640764, compound

https://huagongshe.com/reaction/1003609

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 numberUS06046213
Source datasetuspto-grants-2000_04
ORD IDord-44d8af16ac974090a40b86007c9cf2b8
Source noteuspto-grants-2000_04