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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502547Generated: November 1, 2026

Sodium borohydride → HCID 53257212, compound

https://huagongshe.com/reaction/1502547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86654895HCID 86654895—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53257212HCID 5325721285.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

4-[3′,4′,5′-Tris(octadecyloxy)cyclohexylmethyloxy]-3,5-dimethoxybenzaldehyde (73 mg, 0.07 mmol) was dissolved in THF (2 ml), 4 equivalents of sodium borohydride was added, and the mixture was stirred at 40° C. for 3 hr. The solvent was evaporated, and chloroform was added. The mixture was washed successively with 1N hydrochloric acid, aqueous sodium hydrogen carbonate solution and saturated brine. The solvent of the organic layer was evaporated, and acetonitrile was added. The precipitate was collected by filtration and dried to give 3,5-dimethoxy-4-[3′,4′,5′-tris(octadecyloxy)cyclohexylmethyloxy]benzyl alcohol (70 mg, 0.06 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206230B2
Source datasetuspto-grants-2015_12
ORD IDord-8c436dbeed044e2ba81e5e3f0b2482ad
Source noteuspto-grants-2015_12