Potassium Cation → HCID 178498548, compound

Reaction equation

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

Participants

Reactant 6

HCID 813Potassium Cation2×

HCID 6228Dimethylformamide

HCID 7498Benzyl Bromide

HCID 8857Ethyl Acetate

HCID 19660Carbonate Ion

HCID 67488150Methyl 3-hydroxy-5-(1-hydroxypropan-2-yloxy)benzoate

Product 1

Sources & evidence

ORD record: ord-0ee7daf9df4f44e3b5ebc77ece16c5f8
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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