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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399215Generated: November 1, 2026

Sodium borohydride → HCID 178520638, compound

https://huagongshe.com/reaction/2399215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178520637HCID 178520637—
Solvent1,4-DioxaneHCID 31275—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 178520638HCID 17852063881.3%

Reaction Steps

A solution of 0.44 g of 3-[trans-4-[(4'-fluoro-4-biphenylyl)ethynyl]cyclohexyl]propanal in 20 ml of methanol/water (vol. 4:1) and 15 ml of dioxan is treated portionwise with 0.10 g of sodium borohydride. The reaction mixture is stirred at room temperature for 0.75 hour and concentrated. The residue is treated with water and extracted with diethyl ether. The ether phase is washed with water, dried over sodium sulphate, filtered and evaporated. 0.36 g of 3-[trans-4-[(4'-fluoro-4-biphenylyl)ethynyl]cyclohexyl]propanol is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05447657
Source datasetuspto-grants-1995_09
ORD IDord-3b6163c6f28c4464847990d196772bbb
Source noteuspto-grants-1995_09