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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
Reactant1-Phenyl-2-hexanoneHCID 33191—
ReactantSodium MethoxideHCID 10942334—
Product2-Methyl-3-phenyloctan-4-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410135B2
Source datasetuspto-grants-2013_04
ORD IDord-c83335719a9a4f3b8367bb1aed3f334d
Source noteuspto-grants-2013_04