HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351441Generated: October 25, 2026
Hydrogen Peroxide → 2-(4-Benzyloxy-phenyl)-3-ethyl-5-hydroxymethyl-4-methyl-cyclohexanol
https://huagongshe.com/reaction/351441
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | [4-(4-Benzyloxy-phenyl)-5-ethyl-6-methyl-cyclohex-3-enyl]-methanol | HCID 18436344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | 2-(4-Benzyloxy-phenyl)-3-ethyl-5-hydroxymethyl-4-methyl-cyclohexanol | HCID 18436333 | — |
Reaction Steps
To the solution of [4-(4-benzyloxy-phenyl)-5-ethyl-6-methyl-cyclohex-3-enyl]-methanol (3.1 g, 6.8 mmol) in THF (50 mL) was added BH3.S(CH3)2 solution (1.0 M in THF, 10.3 mL, 1.5 eq.) at 0° C. The reaction mixture was refluxed for 4 h and then cooled to 0° C. NaOH (20% aqueous, 30 mL) and H2O2 (50% in H2O, 21 mL) were added at 0° C. The reaction mixture was then stirred at 0˜25° C. for 4 h. The reaction mixture was then diluted with ethyl acetate/H2O (400 mL/200 mL). The organic layer was separated, dried over MgSO4 and purified on SiO2 (50˜100% ethyl acetate/hexane) to yield 2-(4-benzyloxy-phenyl)-3-ethyl-5-hydroxymethyl-4-methyl-cyclohexanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183445B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-73f1c5ea53c54f169e78a3de55763651 |
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| Source note | uspto-grants-2007_02 |
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