HCID 12397040, compound → HCID 86733479, compound

HRID 1077299Notes

Reaction equation

HRID 1077299 reaction equation
[C:1](OC1C=CC(C)=CC=1O)(=O)C1C=CC=CC=1.C(O[C:27]1[CH:28]=[CH:29][C:30]([OH:39])=[C:31]([CH:38]=1)[O:32][CH2:33][C:34]([NH:36][CH3:37])=[O:35])(=O)C1C=CC=CC=1.C(OC1C=CC(OCC2C=CC=CC=2)=CC=1O)(=O)C1C=CC=CC=1>>[OH:39][C:30]1[CH:29]=[CH:28][C:27]([CH3:1])=[CH:38][C:31]=1[O:32][CH2:33][C:34]([NH:36][CH3:37])=[O:35]

Participants

4

Reactant 3

HCID 12397040HCID 12397040, compoundHCID 21397696HCID 21397696, compoundHCID 86733480HCID 86733480, compound

Product 1

HCID 86733479HCID 86733479, compound

Procedure

2-Hydroxy-N,5-dimethylphenoxyacetamide, m.p. 163°-165°C. is prepared from 2-benzoyloxy-5-methylphenol by a similar process to that described in Example 12 for the preparation of 5-benzoyloxy-2-hydroxy-N-methylphenoxyacetamide from 2-benzoyloxy-5-benzyloxyphenol.

Sources & evidence

ORD record
ord-5cb8136495734262b51e5ff23b73bb4b
Source dataset
uspto-grants-1976_05
Patent number
US03959486

Reaction notes

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