(3-Chloroallyl)benzene → HCID 86735258, compound
Reaction equation
[Cl:1][CH:2]=[CH:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1.C1C(C(OO)=[O:18])=CC=CC=1>C(Cl)(Cl)Cl>[Cl:1][CH:2]=[CH:3][CH2:4][C:5]1[CH:10]2[O:18][CH:9]2[CH:8]=[CH:7][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(a) To 6.1 g of m-chloroallylbenzene was added 85 ml of chloroform solution containing perbenzoic acid and the mixture was allowed to stand at room temperature overnight. This solution was washed with sodium hydroxide solution, 20% Mohr's salt solution and then water, and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain the residue, which was distilled under reduced pressure to give 2.2 g (yield 33%) of m-chloroallylbenzene oxide having a boiling point of 117° C/7 mmHg.
Workup
- washThis solution was washed with sodium hydroxide solution, 20% Mohr's salt solution
- dry with materialwater, and dried over anhydrous sodium sulfate
- customThe solvent was evaporated
- customto obtain the residue, which
- distillationwas distilled under reduced pressure
Sources & evidence
- ORD record
- ord-d1e595a6ebd34d55941ba2e2dd1178dd
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04062862
Reaction notes
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