Benzene → HCID 20332642, compound

HRID 1706880Notes

Reaction equation

HRID 1706880 reaction equation
[Br:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][CH:6]=1)=[O:4].[Cl:12][C:13]1[CH:22]=[CH:21][CH:20]=[CH:19][C:14]=1[CH:15]([OH:18])[CH2:16]O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C1C=CC=CC=1>O.C(O)CCC>[Br:1][CH2:2][C:3]1([C:5]2[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][CH:6]=2)[O:18][CH:15]([C:14]2[CH:19]=[CH:20][CH:21]=[CH:22][C:13]=2[Cl:12])[CH2:16][O:4]1

Participants

7

Reactant 4

HCID 241BenzeneHCID 6101p-Toluenesulfonic acidHCID 68303p-Chlorophenacyl bromideHCID 1010261-(2-Chlorophenyl)ethane-1,2-diol

Product 1

HCID 20332642HCID 20332642, compound

Reagents, catalysts & solvents 2

HCID 2631-ButanolSolventHCID 962WaterSolvent

Procedure

A mixture of 11.5 parts of 2-bromo-p-chloroacetophenone, 10.4 parts of o-chloro-α-(hydroxymethyl)benzylalcohol, 0.2 parts of p-toluenesulfonic acid, 180 parts of benzene and 80 parts of butanol is stirred and refluxed overnight with water-separator. The solvent is removed in vacuo and the residue is dissolved in chloroform. The chloroform solution is stirred with silica gel for 30 minutes. The silica gel is filtered off and the solvent is removed in vacuo, yielding 2-(bromomethyl)-4-(o-chlorophenyl)-2-(p-chlorophenyl)-1,3-dioxolane as a residue.

Workup

  1. customThe solvent is removed in vacuo
  2. dissolutionthe residue is dissolved in chloroform
  3. stirringThe chloroform solution is stirred with silica gel for 30 minutes
  4. filtrationThe silica gel is filtered off
  5. customthe solvent is removed in vacuo

Sources & evidence

ORD record
ord-e326bb5a70844372a9ae775c9b34e4ea
Source dataset
uspto-grants-1980_06
Patent number
US04209447

Reaction notes

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