Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995870Generated: October 31, 2026

1-Chloro-3-methyl-2-butene → HCID 20439306, compound

https://huagongshe.com/reaction/1995870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-3-methyl-2-buteneHCID 10429—
Reactant1-Phenyl-2-butanoneHCID 13879—
ReactantSodium HydroxideHCID 14798—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
ProductHCID 20439306HCID 2043930675%

Reaction Conditions

Temperature60 °C

Reaction Steps

192 g (2.4 mol) of 50% sodium hydroxide and 6 g of hexadecyl-trimethylammonium bromide are placed in a 2-liter flask provided with a thermometer, stirrer and reflux condenser and there is then added dropwise while stirring within 0.5 hour a mixture of 296 g (2 mol) of ethyl benzyl ketone and 251 g (2.4 mol) of prenyl chloride. The mixture is warmed to 60° C. and stirred for 3 hours. The mixture is left to cool and 500 ml of ice/water are added thereto. The mixture is extracted four times with ether and washed neutral with water. The phase separation can be facilitated by the addition of a small amount of alcohol. After drying over sodium sulphate, the ether is evaporated and a fractional distillation is then carried out. There are thus obtained 224 g of 2-methyl-5-phenyl-oct-2-en-6-one of boiling point 106° C./3 mmHg; nD20 =1.5092-88; yield 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04406828
Source datasetuspto-grants-1983_09
ORD IDord-373a6d5ca5e642fc87bf3b267873b2a4
Source noteuspto-grants-1983_09