Chloride → 1-Benzyl-3-bromo-5-chloro-2-pyridone

Reaction equation

[Br:16][CH2:17][c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1.[Br:1][c:2]1[c:3](=[O:9])[nH:4][cH:5][c:6]([Cl:8])[cH:7]1.[C:10](=[O:11])([O-:12])[O-:13].[CH2:25]([N+:26]([CH2:27][CH2:28][CH2:29][CH3:30])([CH2:31][CH2:32][CH2:33][CH3:34])[CH2:35][CH2:36][CH2:37][CH3:38])[CH2:39][CH2:40][CH3:41].[CH3:42][CH2:43][O:44][C:45](=[O:46])[CH3:47].[Cl-:24].[K+:14].[K+:15]>>[Br:1][c:2]1[c:3](=[O:9])[n:4]([CH2:17][c:18]2[cH:19][cH:20][cH:21][cH:22][cH:23]2)[cH:5][c:6]([Cl:8])[cH:7]1

Participants

Reactant 7

HCID 312Chloride

HCID 813Potassium Cation2×

HCID 7498Benzyl Bromide

HCID 8857Ethyl Acetate

HCID 16028Tetrabutylammonium

HCID 19660Carbonate Ion

HCID 27267913-Bromo-5-chloropyridin-2-ol

Product 1

Sources & evidence

ORD record: ord-96d3e713a753455788ab1e1049a18dfa
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Reaction notes

Loading…