HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474257Generated: October 29, 2026
Hydrochloric Acid → HCID 12215290, compound
https://huagongshe.com/reaction/474257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | HCID 178418676 | HCID 178418676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12215290 | HCID 12215290 | 100% |
Reaction Steps
To a 0.5 M solution of 4-fluorophenylmagnesium bromide (298 mL, 149 mmol) in THF at 0° C. was carefully added cyclopentanone (13.23 mL, 149 mmol). Upon the end of the addition, the reaction mixture was heated at reflux for 2 h. Ice (10 g) and 6 N aqueous hydrochloric acid were added. The reaction mixture was extracted with ether. The combined organic extracts were washed with a saturated aqueous solution of sodium hydrogen sulfite, a saturated aqueous solution of sodium bicarbonate and water. The organic layer was dried over anhydrous magnesium sulfate and filtered. The solvent was removed in vacuo and the residue was purified by column chromatography on silica gel to give 1-cyclopentenyl-4-fluorobenzene (24.155 g, 149 mmol, 100% yield) as a colorless oil. LC-MS (M+H)+=163.0. 1H NMR (500 MHz, CDCl3) δ ppm 7.35-7.42 (2H, m), 6.95-7.02 (2H, m), 6.06-6.13 (1H, m), 2.63-2.71 (2H, m), 2.47-2.56 (2H, m), 1.96-2.06 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637523B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-01826b9c56d64f969f1e6e26b3929c0b |
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| Source note | uspto-grants-2014_01 |
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