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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Methyl 3,4,5-tris(octadecyloxy)cyclohexylcarboxylate | HCID 86654892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4,5-Tris(octadecyloxy)cyclohexylmethyl alcohol | HCID 86645785 | 100.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206230B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-9ce10b512c8b4312a476c95852533d07 |
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| Source note | uspto-grants-2015_12 |
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