HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419808Generated: November 2, 2026
Diiodomethane → 4-(1-Methylcyclopropyl)cyclohexanone
https://huagongshe.com/reaction/1419808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(1-Methylethenyl)cyclohexanone | HCID 549291 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(1-Methylcyclopropyl)cyclohexanone | HCID 54101601 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05889012 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-1527b35168534654a5c8f8b41ab5f3a1 |
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| Source note | uspto-grants-1999_03 |
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