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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537608Generated: October 29, 2026

Hydrochloric Acid → 2-Methoxy-4-(2',2',2'-tris(octadecyloxymethyl)ethoxy)benzyl alcohol

https://huagongshe.com/reaction/537608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Methoxy-4-(2',2',2'-tris(octadecyloxymethyl)ethoxy)benzaldehydeHCID 86654890—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-4-(2',2',2'-tris(octadecyloxymethyl)ethoxy)benzyl alcoholHCID 53258810—

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Methoxy-4-(2′,2′,2′-tris(octadecyloxymethyl)ethoxy)benzaldehyde (288 mg, 280 μmol) was dissolved in THF (3 ml), methanol (0.3 ml) and sodium borohydride (31.8 mg, 841 μmol) were added, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was cooled to room temperature, 1N hydrochloric acid (5 ml) and chloroform (5 ml) were added, and the mixture was stirred. The aqueous layer was removed, and the organic layer was further washed twice with purified water (5 ml). The organic layer was evaporated under reduced pressure, and the residue was azeotropically distilled with acetonitrile and dried in vacuo to give 2-methoxy-4-(2′,2′,2′-tris(octadecyloxymethyl)ethoxy)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859732B2
Source datasetuspto-grants-2014_10
ORD IDord-9ffa79220a794fe9ae4cda6444b03c32
Source noteuspto-grants-2014_10