HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537616Generated: October 31, 2026
Sodium borohydride → 2-Methoxy-4-[3',4',5'-tris(octadecyloxy)cyclohexylmethyloxy]benzyl alcohol
https://huagongshe.com/reaction/537616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Methoxy-4-[3',4',5'-tris(octadecyloxy)cyclohexylmethyloxy]benzaldehyde | HCID 86654894 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | 2-Methoxy-4-[3',4',5'-tris(octadecyloxy)cyclohexylmethyloxy]benzyl alcohol | HCID 53257211 | 96.2% |
Reaction Steps
2-Methoxy-4-[3′,4′,5′-tris(octadecyloxy)cyclohexylmethyloxy]benzaldehyde (272 mg, 0.26 mmol) was suspended in chloroform-methanol (6 ml+0.5 ml), and sodium borohydride (29 mg, 0.77 mmol) was added. After stirring at 60° C. overnight, the mixture was dissolved in chloroform (12 ml), and washed with 0.5N hydrochloric acid (8 ml) and pure water (8 ml). The solvent was evaporated, and the residue was precipitated with acetonitrile (2.5 ml) to give 2-methoxy-4-[3′,4′,5′-tris(octadecyloxy)cyclohexylmethyloxy]benzyl alcohol (260 mg, 0.25 mmol, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859732B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f464ef4eec624d8faf7d07a5ccff2f15 |
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| Source note | uspto-grants-2014_10 |
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