Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383226Generated: October 26, 2026

1-(4-Chlorophenyl)-1-cyclopropyl-2-propen-1-ol → HCID 57191402, compound

https://huagongshe.com/reaction/1383226

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Chlorophenyl)-1-cyclopropyl-2-propen-1-olHCID 15042033—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductHCID 57191402HCID 5719140234.3%

Reaction Steps

To a stirred solution of 40.3 grams (0.192 mole) of pyridinium chlorochromate in 210 mL of methylene chloride was added a solution of 20.0 grams (0.096 mole) of 1-(4-chlorophenyl)-1-cyclopropyl-2-propen-1-ol in 25 mL of methylene chloride in one portion. Upon completion of addition, the reaction mixture was stirred for two hours. A supernatent layer was decanted from a residue, and the residue was extracted with diethyl ether. The supernatent layer was combined with the ether extracts, and the combination was washed with two 100 mL portions of an aqueous 5% sodium hydroxide solution, 100 mL of an aqueous 5% hydrochloric acid solution, and then with 50 mL of an aqueous solution saturated with sodium bicarbonate. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel. Elution was accomplished using 5% diethyl ether in hexane. The appropriate fractions were combined and concentrated under reduced pressure, yielding 6.8 grams of 3-(4-chlorophenyl)-3-cyclopropylpropenal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808762
Source datasetuspto-grants-1989_02
ORD IDord-b0dfcf1920a74385b523eea6d4a4a975
Source noteuspto-grants-1989_02