HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719123Generated: November 1, 2026
Water → 1-(4-Chloro-phenyl)-3-cyclopentyl-propan-1-one
https://huagongshe.com/reaction/719123
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | 3-Cyclopentylpropionyl chloride | HCID 66039 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-(4-Chloro-phenyl)-3-cyclopentyl-propan-1-one | HCID 21896900 | 25.3% |
Reaction Steps
Aluminum chloride (4.979 g, 37.34 mmol) was added in small portions to a solution of 3-cyclopentylpropionyl chloride (3 g, 18.67 mmol) in 1,2-dichloroethane (100 mL) cooled to 0° C. After 15 min., chlorobenzene (6.304 g, 56.01 mmol) was added. The reaction mixture was stirred at 0° C. for 1 h and at room temperature for 48 h. It was then poured into a mixture of ice and water. The product was extracted with ethyl acetate. The organic layers were washed with saturated solution of sodium bicarbonate (1×30 mL), brine (1×20 mL) and dried over anhydrous magnesium sulfate. The solids were then filtered off, and the filtrate was concentrated in vacuo. Purification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32–63 μm, 60 Å silica gel) eluting with hexanes yielded 1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one (1.12 g, 25%) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07132421B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-b409d5c049e44fc9b3ee480d00d8fc9b |
|---|
| Source note | uspto-grants-2006_11 |
|---|