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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271840Generated: October 25, 2026

Tetrahydrofuran → 2-Phenethyl-cyclohexanone

https://huagongshe.com/reaction/271840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Chloro-2-phenylethaneHCID 231496—
ReactantCID 53628100HCID 178418400—
Product2-Phenethyl-cyclohexanoneHCID 231615—

Reaction Conditions

Temperature-78 °C

Reaction Steps

s-BuLi (28.0 mL, 1.3 M) was added slowly to a solution of Compound 20b (7.0 g) in THF (50 mL) at −78° C. The mixture stirred for 1 hr at −78° C. and then (2-chloro-ethyl)-benzene Compound 20c (5.11 g, 36.4 mmol) in THF (10 mL) was added dropwise. The reaction mixture was stirred for 24 hrs while warming to r.t. The reaction was quenched with 1N HCl (5 mL), then diluted with water (100 mL) and EtOAc (500 mL). The organic layer was washed with brine, separated and dried with anhydrous sodium sulfate, then filtered and concentrated in vacuo to yield a crude product. Purification by flash chromatography (eluted with 10% EtOAc in Hexane) afforded 2-phenethyl-cyclohexanone Compound 20d (4.05 g, 20.0 mMol, 58%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452997B2
Source datasetuspto-grants-2008_11
ORD IDord-5e24323ad1164353bd8e9c877b49b9ce
Source noteuspto-grants-2008_11