Potassium Cation → 2-Amino-2'-benzyloxy-5-chlorobenzophenone

Reaction equation

[Br:24][CH2:25][c:26]1[cH:27][cH:28][cH:29][cH:30][cH:31]1.[C:18](=[O:19])([O-:20])[O-:21].[CH3:32][N:33]([CH3:34])[CH:35]=[O:36].[K+:22].[K+:23].[NH2:1][c:2]1[c:3]([C:4](=[O:5])[c:6]2[c:7]([OH:12])[cH:8][cH:9][cH:10][cH:11]2)[cH:13][c:14]([Cl:17])[cH:15][cH:16]1>>[NH2:1][c:2]1[c:3]([C:4](=[O:5])[c:6]2[c:7]([O:12][CH2:25][c:26]3[cH:27][cH:28][cH:29][cH:30][cH:31]3)[cH:8][cH:9][cH:10][cH:11]2)[cH:13][c:14]([Cl:17])[cH:15][cH:16]1

Participants

Reactant 5

HCID 813Potassium Cation2×

HCID 6228Dimethylformamide

HCID 7498Benzyl Bromide

HCID 19660Carbonate Ion

HCID 5264882-Amino-5-chloro-2'-hydroxybenzophenone

Product 1

HCID 541754792-Amino-2'-benzyloxy-5-chlorobenzophenone

Sources & evidence

ORD record: ord-aee1d73f559a431dbe855901eab912ba
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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