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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003607Generated: October 30, 2026

Sodium borohydride → HCID 70236260, compound

https://huagongshe.com/reaction/1003607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21186591HCID 21186591—
SolventEthanolHCID 702—
ProductHCID 70236260HCID 7023626056.7%

Reaction Steps

A mixture of sodium borohydride (0.054 g, 1.43 mmol) and ethanol (5 mL) was stirred 10 min and then 1-(3,5-dimethyl-4-triisopropylsilyloxyphenyl)-2-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)-propan-1-one (0.77 g, 1.42 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 0.44 g (56%) of (1R*,2R*)-1-(3,5-dimethy-4-triisopropylsilyloxyphenyl)-2-(4-(4-chlorophenyl)-4-hydroxypiperdin-1-yl)-propan-1-ol which was suitable for use without further purification and had: mp 211.5-212.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046213
Source datasetuspto-grants-2000_04
ORD IDord-205f6e19249b437d9c708ec9f7dcb661
Source noteuspto-grants-2000_04