Triphenylphosphine → HCID 20285675, compound

HRID 904486Notes

Reaction equation

HRID 904486 reaction equation
[Cl:1][CH2:2][C:3]1[C:7]([CH3:8])=[C:6]([Cl:9])[S:5][C:4]=1[Cl:10].[C:11]1([P:17]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C1C=CC=CC=1>[Cl-:1].[Cl:10][C:4]1[S:5][C:6]([Cl:9])=[C:7]([CH3:8])[C:3]=1[CH2:2][P+:17]([C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1

Participants

4

Reactant 2

HCID 11776TriphenylphosphineHCID 20285690HCID 20285690, compound

Product 1

HCID 20285675HCID 20285675, compound

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

A mixture of 25.4 g. (0.12 mol) of 3-chloromethyl-2,5-dichloro-4-methylthiophene, 34.6 g. (0.132 mol) of triphenylphosphine and 200 ml. of benzene was heated to the reflux overnight. The resulting beige solid was filtered to yield (2,5-dichloro-4-methyl-3-thenyl)-triphenylphosphonium chloride, m.p. 238°-240° C.

Workup

  1. additionA mixture of 25.4 g
  2. filtrationThe resulting beige solid was filtered

Sources & evidence

ORD record
ord-9c778e52c4ef48e8802f9aa1a338f06d
Source dataset
uspto-grants-1980_10
Patent number
US04230872

Reaction notes

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