Isophthaloyl chloride → HCID 54397727, compound

HRID 2309569Notes

Reaction equation

[OH:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[O:7])=[CH:4][CH:3]=1.[C:19](Cl)(=[O:29])[C:20]1[CH:28]=[CH:27][CH:26]=[C:22]([C:23](Cl)=[O:24])[CH:21]=1>>[CH2:9]([O:8][C:6]([C:5]1[CH:4]=[CH:3][C:2]([O:1][C:19](=[O:29])[C:20]2[CH:28]=[CH:27][CH:26]=[C:22]([C:23]([O:1][C:2]3[CH:3]=[CH:4][C:5]([C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[O:7])=[CH:17][CH:18]=3)=[O:24])[CH:21]=2)=[CH:18][CH:17]=1)=[O:7])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]

Participants

Reactant 2

HCID 7451Isophthaloyl chloride

HCID 14642Octylparaben

Product 1

HCID 54397727HCID 54397727, compound

Procedure

Octyl p-hydroxybenzoate and isophthalic dichloride are made to react and treated in a similar procedure to Example 4 to yield di(p-octyloxycarbonylphenyl)isophthalate in a pale yellow oily state.

Workup

customto react
additiontreated in a similar procedure to Example 4

Sources & evidence

ORD record: ord-5f134a62915a4297ba5c748d04266bef
Source dataset: uspto-grants-1987_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04695649

Reaction notes

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