Potassium Cation → 2-n-Butyl-4-chloro-1-(4-bromobenzyl)-5-formylimidazole

HRID 2127183Notes

Reaction equation

HRID 2127183 reaction equation
[Br:13][c:14]1[cH:15][cH:16][c:17]([CH2:18][Br:19])[cH:20][cH:21]1.[C:22](=[O:23])([O-:24])[O-:25].[CH2:1]([CH2:2][CH2:3][CH3:4])[c:5]1[nH:6][c:7]([CH:11]=[O:12])[c:8]([Cl:10])[n:9]1.[CH3:28][N:29]([CH3:30])[C:31](=[O:32])[CH3:33].[CH3:34][c:35]1[cH:36][cH:37][cH:38][cH:39][cH:40]1.[K+:26].[K+:27].[OH2:41]>>[CH2:1]([CH2:2][CH2:3][CH3:4])[c:5]1[n:6]([CH2:18][c:17]2[cH:16][cH:15][c:14]([Br:13])[cH:21][cH:20]2)[c:7]([CH:11]=[O:12])[c:8]([Cl:10])[n:9]1

Participants

8

Reactant 7

HCID 813Potassium Cation2×HCID 962WaterHCID 1140TolueneHCID 19660Carbonate IonHCID 31374DimethylacetamideHCID 685274-Bromobenzyl bromideHCID 178418251HCID 178418251, compound

Product 1

HCID 99505572-n-Butyl-4-chloro-1-(4-bromobenzyl)-5-formylimidazole

Sources & evidence

ORD record
ord-cbba550a2e55423ebde271ceaef66f9c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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