1-Chloro-3-methyl-2-butene → 52750-95-5

HRID 1155667Notes

Reaction equation

HRID 1155667 reaction equation
[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][Cl:5].[C:7]1([P:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C1(C)C=CC=CC=1>[Cl-:5].[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][P+:13]([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Participants

4

Reactant 2

HCID 104291-Chloro-3-methyl-2-buteneHCID 11776Triphenylphosphine

Product 1

HCID 1895455552750-95-5Yield 80.5%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A stirred solution of 52.3 g (0.5 mole) of 3-methyl-2-butenyl chloride and 144.1 g (0.55 mole) of triphenylphosphine in 400 ml of toluene was heated at 100° C. for 18 hours. The white solid formed was collected by filtration to give 147.6 g of (3-methyl-2-butenyl)triphenylphosphonium chloride.

Workup

  1. customThe white solid formed
  2. filtrationwas collected by filtration

Sources & evidence

ORD record
ord-5fcfdb11168b43eaaa19e790f8214bb8
Source dataset
uspto-grants-1982_06
Patent number
US04332815

Reaction notes

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