HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093Generated: October 26, 2026
Methyl 12-hydroxystearate → Hydroxystearyl alcohol
https://huagongshe.com/reaction/1093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 12-hydroxystearate | HCID 8840 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Hydroxystearyl alcohol | HCID 95421 | 86.6% |
Reaction Steps
A 5-liter flask equipped with a stirrer, dropping funnel and reflux tube was charged with 28.5 g (0.75 mol) of LiAlH4 and 2 liters of tetrahydrofuran, to which a solution of 237.0 g (0.75 mol) of methyl 12-hydroxyoctadecanate in 1 liter of tetrahydrofuran was added dropwise over 5 hours with stirring. After completion of the dropping, the stirring was continued further for 1 hour at 65° C. After the reaction mixture was then cooled, 90 ml of a 5% aqueous solution of KOH were added with stirring. A salt precipitated was separated by filtration, and the resultant solution was concentrated under reduced pressure. The resulting residue was purified by column chromatography on silica gel, thereby obtaining 185.7 g (yield: 86.6%) of 1,12-octadecanediol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723497 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-9598dbc5228f4c2bae79065911c76e2b |
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| Source note | uspto-grants-1998_03 |
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