Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382702Generated: October 31, 2026

Sodium borohydride → HCID 53828330, compound

https://huagongshe.com/reaction/1382702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22222788HCID 22222788—
SolventMethanolHCID 887—
ProductHCID 53828330HCID 53828330—

Reaction Steps

0.57 g of sodium borohydride is added in portions, over a period of 15 minutes, to a stirred solution of 9.3 g of 2-nonylbenzaldehyde in 150 ml of methanol. After stirring for a further 30 minutes, the reaction mixture is concentrated by evaporation under reduced pressure and the residue is taken up in ether. The organic phase is washed with ice-cooled 0.2N hydrochloric acid and with water, dried over sodium sulphate and concentrated by evaporation in vacuo. Chromatographic purification of the residue on silica gel with mixtures of petroleum ether with an increasing amount of ether yields 2-nonylbenzyl alcohol in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808572
Source datasetuspto-grants-1989_02
ORD IDord-4d6adc833946441f9933e1fde97b7288
Source noteuspto-grants-1989_02