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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405668Generated: November 1, 2026

6-Methyl-5-hepten-2-one → HCID 86675567, compound

https://huagongshe.com/reaction/2405668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methyl-5-hepten-2-oneHCID 9862—
ReactantCrotyl chlorideHCID 11589—
ReactantPotassium HydroxideHCID 14797—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventTolueneHCID 1140—
ProductHCID 86675567HCID 86675567—

Reaction Conditions

Temperature70 °C

Reaction Steps

In a 1 liter 4-necked flask, equipped with a mechanical stirrer, 6-methylhept-5-en-2-one (126.81 g, 1.00 mol) was dissolved in toluene (125 ml). An aqueous solution of KOH (45%, 354.15 g, 2.84 mol) was added at room temperature. The biphasic mixture was heated to 70° C. under stirring. A solution of PTC catalyst (trioctyl methyl ammonium chloride, Aliquat 336, 6.46 g, 16 mmol), and crotyl chloride (136.4 g, 1.51 mol) in toluene (10.0 g) was then added over 2.5 hours at 70° C. The mixture was then cooled to room temperature and stirred overnight. A partial conversion into the desired compound was observed. The crude reaction mixture was poured onto water (250 ml), and washed successively with aqueous H3PO4 (12.5%, 400 ml), aqueous NaCl (15%, 250 ml), NaHCO3 (5%, 100 ml) and 3 times with aqueous NaCl (25%, 100 ml). After drying over Na2SO4 and filtration, the solvent was removed in vacuuo. The concentrated product was distilled through a Vigreux column A second distillation through a Fischer column afforded the desired product (as a 4/1 mixture of E and Z isomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809256B2
Source datasetuspto-grants-2014_08
ORD IDord-e97eb87afd28418aba6113c4861a9d2c
Source noteuspto-grants-2014_08