Hydroquinone → HCID 20346515, compound

HRID 1701769Notes

Reaction equation

HRID 1701769 reaction equation
[C:1]1([C:7]2[O:8][CH2:9][CH2:10][N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:12]1([CH:19]=[CH:18][C:16]([OH:17])=[CH:15][CH:14]=1)[OH:13]>>[C:7]([NH:11][CH2:10][CH2:9][O:13][C:12]1[CH:19]=[CH:18][C:16]([O:17][CH2:9][CH2:10][NH:11][C:7](=[O:8])[C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:15][CH:14]=1)(=[O:8])[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 785HydroquinoneHCID 2440302-Phenyl-2-oxazoline

Product 1

HCID 20346515HCID 20346515, compound

Procedure

In German Pat. No. 1,062,253, A. Jager describes the preparation of various ether and carboxamide compounds by treating certain substituted oxazolines with certain phenols, with the exclusion of water. A mixture of phenol and 2-phenyloxazoline refluxed for 7 hours yielded PhCONHCH2CH2OPh as a product. Similarly, p-bis(oxazolinyl)benzene and phenol gave N,N'-bis(β-phenoxyethyl)terephthalamide. Finally, Jager found that a mixture of 2-phenyl-2-oxazoline and hydroquinone produced 1,4-bis(β-benzamidoethoxy)benzene.

Sources & evidence

ORD record
ord-041c5c06cb3b49cda0f6f4633e5c9f5c
Source dataset
uspto-grants-1980_03
Patent number
US04195154

Reaction notes

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