HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874312Generated: October 26, 2026
Methanol → 1-[Cyano(p-benzyloxyphenyl)methyl]cyclohexanol
https://huagongshe.com/reaction/1874312
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Benzyloxyphenylacetonitrile | HCID 522804 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-[Cyano(p-benzyloxyphenyl)methyl]cyclohexanol | HCID 46186538 | 83.9% |
Reaction Steps
p-Benzyloxyphenyl acetonitrile (100 g) and methanol (300 ml) was charged into flask Subsequently the reaction mixture was cooled to 0-5° C. and 10% aqueous solution of sodium hydroxide (180 g) and PEG-400 (10 ml) were added. The reaction mixture was then stirred for 30 min. and cyclohexanone (64 g) was added dropwise at 0-5° C. Subsequently, the reaction mass temperature was raised to 25-27° C. and stirred for 15 hours. After completion of the reaction hexane (600 ml) was added, the reaction mixture filtered, washed with hexane (100 ml) followed by DM water to obtain 120 g (83.9%) of the 1-[cyano(p-benzyloxyphenyl)methyl]cyclohexanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304578B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-eb37c6964c4e4ae6bb3bf303618c0387 |
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| Source note | uspto-grants-2012_11 |
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