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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741837Generated: November 1, 2026

Butyl iodide → HCID 19010813, compound

https://huagongshe.com/reaction/1741837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
Reactant2-Methoxy-4-(2-methyl-1-propen-1-yl)benzoyl chlorideHCID 19010811—
CatalystZinc copper coupleHCID 10290809—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
ProductHCID 19010813HCID 1901081360.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-iodobutane (185 mg) and zinc-copper couple (101 mg) in benzene (3 ml) and N,N-dimethylformamide (0.2 ml) was stirred at 60° C. for 2 hours. To the mixture, a solution of tetrakis(triphenylphosphine)palladium (31 mg) and 2-methoxy-4-(2-methyl-1-propenyl)benzoyl chloride (prepared from 138 mg of 2-methoxy-4-(2-methyl-1propenyl)benzoic acid and 0.07 ml of oxalyl chloride) in benzene (2 ml) was added, and the reaction mixture was stirred at room temperature for 30 minutes. The mixture was filtered and the filtrate was concentrated. The residue was dissolved in ethyl acetate and the organic solution was washed with water and brine, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel column eluting with a mixture of hexane and ethyl acetate (9:1) to give 2'-methoxy-4'-(2-methyl-1-propenyl)valerophenone (91 mg) 10 as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334716
Source datasetuspto-grants-1994_08
ORD IDord-083f3233553d4dbfa3c7d233603f8751
Source noteuspto-grants-1994_08