Dichloromethane → 4-Octyl-biphenyl-4'-terephthalic acid chloride

HRID 21426

Reaction equation

HRID 21426 reaction equation
O[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[C:22]([Cl:33])(=[O:32])[C:23]1[CH:31]=[CH:30][C:26]([C:27]([Cl:29])=[O:28])=[CH:25][CH:24]=1.ClCCl.CN(C1C=CC=CN=1)C>C(N(CC)CC)C>[CH2:14]([C:11]1[CH:10]=[CH:9][C:8]([C:5]2[CH:4]=[CH:3][C:2]([C:31]3[C:23]([C:22]([Cl:33])=[O:32])=[CH:24][CH:25]=[C:26]([C:27]([Cl:29])=[O:28])[CH:30]=3)=[CH:7][CH:6]=2)=[CH:13][CH:12]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]

Participants

6

Procedure

To a solution of 4-hydroxy-4'-octylbiphenyl (0.5 g) and terephthaloyl chloride (0.36 g) in about dichloromethane (30 ml) was added drop by drop triethylamine (0.2 g). To the solution was added dimethylaminopyridine (0.013 g) and the mixture was stirred at the room temperature for 10 hours to obtain the titled compound.

Sources & evidence

ORD record
ord-2394b2dec9d049a3b2e5b53f9d321778
Source dataset
uspto-grants-1995_06
Patent number
US05424005

Linked notes

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