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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351442Generated: October 31, 2026

HCID 18436340, compound → HCID 18436339, compound

https://huagongshe.com/reaction/351442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18436340HCID 18436340—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 18436339HCID 18436339—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183445B2
Source datasetuspto-grants-2007_02
ORD IDord-b7a0700f32af4ba6a2e557f1f692cc61
Source noteuspto-grants-2007_02