HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958558Generated: October 31, 2026
Isopropyl iodide → 2-Methyl-3-phenyloctan-4-one
https://huagongshe.com/reaction/1958558
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | 1-Phenyl-2-hexanone | HCID 33191 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Product | 2-Methyl-3-phenyloctan-4-one | HCID 59864985 | — |
Reaction Steps
To an ice-cold magnetically stirred mixture of 1-phenylhexan-2-one (Intermediate II-1) (7.04 gram, 0.04 mol) and sodium methoxide (4.32 g, 0.08 mol) was added dropwise 2-iodopropane (15 ml) in a nitrogen atmosphere. The resulting mixture was heated for 1 hour at reflux temperature. The obtained mixture was allowed to attain room temperature and concentrated. The resulting residue was taken up in diethyl ether and water. The diethyl ether layer was separated and successively washed with an aqueous Na2S2O3 solution and water. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was further purified using Sepacore equipment: (petroleum ether/diethyl ether=19/1 (v/v)) to give 2-methyl-3-phenyl-octan-4-one (Intermediate IIa-1) (3.52 gram) as a colorless oil; 1H-NMR (400 MHz, CDCl3) δ 0.66 (d, J=7, 3H), 0.81 (t, J=7, 3H), 0.96 (d, J=7, 3H), 1.10-1.24 (m, 2H), 1.36-1.54 (m, 2H), 2.29-2.47 (m, 3H), 3.30 (d, J=10 Hz, 1H), 7.20-7.33 (m, 5H). Rf (petroleum ether/diethyl ether=98/2 (v/v))˜0.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410135B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-c83335719a9a4f3b8367bb1aed3f334d |
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| Source note | uspto-grants-2013_04 |
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