HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789991Generated: October 29, 2026
Cyclohexanecarbonyl chloride → Cyclohexyl 2-Fluorobenzyl Ketone
https://huagongshe.com/reaction/1789991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | HCID 178505630 | HCID 178505630 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | Cyclohexyl 2-Fluorobenzyl Ketone | HCID 22037180 | — |
Reaction Steps
To a mixture of 36 ml of 2-fluorobenzylzinc chloride (0.5 M sol. in tetrahydrofuran) and 0.008 g of dichlorobis(triphenylphosphine)palladium(II) stirred at 0° C. was added dropwise via a syringe 2.14 ml of cyclohexanecarbonyl chloride. Afterwards, the reaction mixture was stirred at r.t. for 4 h, quenched with an aqueous saturated solution of ammonium chloride (25 ml), extracted with 20 ml of EtOAc, which was dried (Na2SO4) and evaporated to dryness in vacuo affording 3.52 g of the title compound as a crude, which could be used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071197B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-ee37b3bbe8884342a72654bff4d2cc0e |
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| Source note | uspto-grants-2006_07 |
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