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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537616Generated: October 31, 2026

Sodium borohydride → 2-Methoxy-4-[3',4',5'-tris(octadecyloxy)cyclohexylmethyloxy]benzyl alcohol

https://huagongshe.com/reaction/537616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Methoxy-4-[3',4',5'-tris(octadecyloxy)cyclohexylmethyloxy]benzaldehydeHCID 86654894—
SolventChloroformHCID 6212—
SolventChloroform methanolHCID 21584188—
Product2-Methoxy-4-[3',4',5'-tris(octadecyloxy)cyclohexylmethyloxy]benzyl alcoholHCID 5325721196.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Methoxy-4-[3′,4′,5′-tris(octadecyloxy)cyclohexylmethyloxy]benzaldehyde (272 mg, 0.26 mmol) was suspended in chloroform-methanol (6 ml+0.5 ml), and sodium borohydride (29 mg, 0.77 mmol) was added. After stirring at 60° C. overnight, the mixture was dissolved in chloroform (12 ml), and washed with 0.5N hydrochloric acid (8 ml) and pure water (8 ml). The solvent was evaporated, and the residue was precipitated with acetonitrile (2.5 ml) to give 2-methoxy-4-[3′,4′,5′-tris(octadecyloxy)cyclohexylmethyloxy]benzyl alcohol (260 mg, 0.25 mmol, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859732B2
Source datasetuspto-grants-2014_10
ORD IDord-f464ef4eec624d8faf7d07a5ccff2f15
Source noteuspto-grants-2014_10