HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351442Generated: October 31, 2026
HCID 18436340, compound → HCID 18436339, compound
https://huagongshe.com/reaction/351442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18436340 | HCID 18436340 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 18436339 | HCID 18436339 | — |
Reaction Steps
To a solution of 3-ethyl-4-methyl-2-(4-phenoxy-phenyl)-5-trimethylsilanyloxymethyl-cyclohexanone (1.8 g, 3.8 mmol) in THF (10 mL) at −10° C. was added Grinard reagent (1.0 M, 7.5 mL). The reaction mixture was stirred at 25° C. for 1 h and then refluxed for 30 min. The reaction mixture was then cooled and diluted with aqueous saturated NH4Cl (100 mL) and ethyl acetate (100 mL). The organic layer was separated, dried over MgSO4 and purified on SiO2 (100% ethyl acetate) to yield crude product 3-ethyl-1-(4-methoxy-phenyl)-4-methyl-2-(4-phenoxy-phenyl)-5-trimethylsilanyloxymethyl-cyclohexanol. NMR showed S: R product ratio or 2:1. Further purification provide pure 3-ethyl-1-(4-methoxy-phenyl)-4-methyl-2-(4-phenoxy-phenyl)-5-trimethylsilanyloxymethyl-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-b7a0700f32af4ba6a2e557f1f692cc61 |
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| Source note | uspto-grants-2007_02 |
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