HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271840Generated: October 25, 2026
Tetrahydrofuran → 2-Phenethyl-cyclohexanone
https://huagongshe.com/reaction/271840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Chloro-2-phenylethane | HCID 231496 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Product | 2-Phenethyl-cyclohexanone | HCID 231615 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452997B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-5e24323ad1164353bd8e9c877b49b9ce |
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| Source note | uspto-grants-2008_11 |
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