Phosphorus tribromide → (6-Bromohex-3-en-1-yl)benzene

HRID 1703962Notes

Reaction equation

HRID 1703962 reaction equation
[C:1]1([CH2:7][CH2:8][CH:9]([CH:11]2[CH2:13][CH2:12]2)O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Br)(Br)[Br:15].[Br-].[Li+]>[Br-].[Zn+2].[Br-]>[C:1]1([CH2:7][CH2:8][CH:9]=[CH:11][CH2:12][CH2:13][Br:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

5

Reactant 3

HCID 24614Phosphorus tribromideHCID 82050Lithium BromideHCID 10899201HCID 10899201, compound

Product 1

HCID 53420932(6-Bromohex-3-en-1-yl)benzene

Reagents, catalysts & solvents 1

HCID 10421208Zinc bromideCatalyst

Procedure

6-Phenyl-3-hexenyl bromide [V; Ar is C6H5, R is H] was prepared from 16.5 g. of 2-phenylethyl cyclopropyl carbinol (Preparation B6), 21.5 g. of phosphorus tribromide, 17.65 g. of lithium bromide and 20.7 g. of zinc bromide according to the procedure given above in Preparation C1, affording 21 g. of product as a pale yellow oil.

Workup

  1. customaffording 21 g

Sources & evidence

ORD record
ord-6a9bd3a27ed3447daf9ff8321e4a3419
Source dataset
uspto-grants-1978_11
Patent number
US04125541

Reaction notes

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