HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383225Generated: October 26, 2026
4-Chlorophenyl cyclopropyl ketone → 1-(4-Chlorophenyl)-1-cyclopropyl-2-propen-1-ol
https://huagongshe.com/reaction/1383225
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorophenyl cyclopropyl ketone | HCID 81148 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Chlorophenyl)-1-cyclopropyl-2-propen-1-ol | HCID 15042033 | — |
Reaction Steps
A 1.0 M solution of vinylmagnesium bromide in tetrahydrofuran (110 mL, 0.11 mole) was stirred, and a solution of 18.1 grams (0.1 mole) of commercially available 4-chlorophenyl cyclopropyl ketone in 50 mL of dry tetrahydrofuran was added dropwise during a one hour period. The exothermic reaction caused the reaction mixture to warm to 45° C. Upon completion of addition, the reaction mixture was stirred for two hours as it cooled to ambient temperature. The reaction was quenched with the addition of 50 mL of a saturated, aqueous solution of ammonium chloride. The mixture was extracted with two 50 mL portions of diethyl ether. The combined extracts were dried with potassium carbonate and filtered. The filtrate was concentrated under reduced pressure, yielding 20.0 grams of 1-(4-chlorophenyl)-1-cyclopropyl-2-propen-1-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04808762 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-e78e86f079834794837be085a611ea67 |
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| Source note | uspto-grants-1989_02 |
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