Acetone → HCID 18673278, compound

HRID 160341Notes

Reaction equation

HRID 160341 reaction equation
[Br-:29].[Br:21][CH2:22][c:23]1[cH:24][cH:25][cH:26][cH:27][cH:28]1.[C:15](=[O:16])([O-:17])[O-:18].[CH3:30][CH2:31][CH2:32][CH2:33][N+:34]([CH2:35][CH2:36][CH2:37][CH3:38])([CH2:39][CH2:40][CH2:41][CH3:42])[CH2:43][CH2:44][CH2:45][CH3:46].[CH3:47][C:48](=[O:49])[CH3:50].[Cl:1][c:2]1[c:3]([N+:12](=[O:13])[O-:14])[cH:4][c:5]2[c:6]([nH:7][c:8](=[O:10])[o:9]2)[cH:11]1.[K+:19].[K+:20]>>[Cl:1][c:2]1[c:3]([N+:12](=[O:13])[O-:14])[cH:4][c:5]2[c:6]([n:7]([CH2:22][c:23]3[cH:24][cH:25][cH:26][cH:27][cH:28]3)[c:8](=[O:10])[o:9]2)[cH:11]1

Participants

8

Reactant 7

HCID 180AcetoneHCID 259Bromide ionHCID 813Potassium Cation2×HCID 7498Benzyl BromideHCID 16028TetrabutylammoniumHCID 19660Carbonate IonHCID 2415982(3h)-benzoxazolone, 5-chloro-6-nitro-

Product 1

HCID 18673278HCID 18673278, compound

Sources & evidence

ORD record
ord-a2a43f151a454e15b3694f0d370f1f67
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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