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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419808Generated: November 2, 2026

Diiodomethane → 4-(1-Methylcyclopropyl)cyclohexanone

https://huagongshe.com/reaction/1419808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(1-Methylethenyl)cyclohexanoneHCID 549291—
ReactantHCID 178418750HCID 178418750—
SolventHexaneHCID 8058—
Product4-(1-Methylcyclopropyl)cyclohexanoneHCID 54101601—

Reaction Conditions

Temperature-60 °C

Reaction Steps

5.0 g (0.036 mol) of 4-isopropenylcyclohexanone (precursor to Example 4) were placed under inert gas in 150 ml of hexane, and 16.5 g (0.134 mol) of diethylzinc (1M in hexane) followed by 58.0 g (0.22 mol) of diiodomethane were added dropwise at -20° C. The mixture was stirred at -60° C. for 2 hours and then at 0° C. for 6 hours. The reaction solution was kept in a refrigerator overnight and was worked up by pouring it into cold NH4Cl solution and carrying out extraction with ether. The organic phase was washed with sodium thiosulfate solution and water, dried and concentrated. 5.3 g (96% of theory) of a colorless oil were obtained which was reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889012
Source datasetuspto-grants-1999_03
ORD IDord-1527b35168534654a5c8f8b41ab5f3a1
Source noteuspto-grants-1999_03