3-amino-4-chlorobenzophenone → HCID 20324253, compound

HRID 441359Notes

Reaction equation

HRID 441359 reaction equation
NC1C=C(C=CC=1Cl)C(C1C=CC=CC=1)=O.[N+:17]([C:20]1[CH:21]=[C:22]([CH:33]=[CH:34][C:35]=1[Cl:36])[C:23]([CH2:31][CH3:32])([OH:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)([O-])=O>>[NH2:17][C:20]1[CH:21]=[C:22]([CH:33]=[CH:34][C:35]=1[Cl:36])[C:23]([CH2:31][CH3:32])([OH:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

Participants

3

Reactant 2

HCID 107995483-amino-4-chlorobenzophenoneHCID 203242573-Nitro-4-chloro-alpha-ethyl-benzhydrol

Product 1

HCID 20324253HCID 20324253, compound

Procedure

This compound is prepared from 3-amino-4-chlorobenzophenone as described in Example 1, or by reducing 3-nitro-4-chloro-α-ethyl-benzhydrol as described in Example 7. The product melts at 103° C.

Sources & evidence

ORD record
ord-1d313d89ee1244d7bdd18942a6b1cf4d
Source dataset
uspto-grants-1977_08
Patent number
US04039589

Reaction notes

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