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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502541Generated: October 25, 2026

Hydrochloric Acid → 3,4,5-Tris(octadecyloxy)cyclohexylmethyl alcohol

https://huagongshe.com/reaction/1502541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantMethyl 3,4,5-tris(octadecyloxy)cyclohexylcarboxylateHCID 86654892—
SolventTetrahydrofuranHCID 8028—
Product3,4,5-Tris(octadecyloxy)cyclohexylmethyl alcoholHCID 86645785100.4%

Reaction Steps

Methyl 3,4,5-tris(octadecyloxy)cyclohexylcarboxylate (70.0 g, 73.9 mmol) was dissolved in THF (1050 ml), and DIBAL (1.0 mol/L toluene solution, 200 ml, 200 mmol) was added dropwise at 0° C. over 40 min under a nitrogen atmosphere. After stirring at room temperature for 2 hr, 0.2N hydrochloric acid (50 ml) was added dropwise at 0° C. to quench the reaction. The solvent was evaporated to about half, and the residue was dissolved in chloroform (700 ml). The mixture was washed three times with 1N hydrochloric acid (300 ml), once with 5% aqueous sodium hydrogen carbonate solution (300 ml), and once with 20% brine (300 ml). The solvent was evaporated, and the residue was precipitated with methanol (700 ml), and washed with acetonitrile to give 3,4,5-tris(octadecyloxy)cyclohexylmethyl alcohol (68.2 g, 74.2 mmol, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206230B2
Source datasetuspto-grants-2015_12
ORD IDord-9ce10b512c8b4312a476c95852533d07
Source noteuspto-grants-2015_12