Carbon Dioxide → HCID 13924302, compound

HRID 2330282Notes

Reaction equation

HRID 2330282 reaction equation
[C:34](=[O:35])([O-:36])[O-:37].[CH3:44][CH2:45][O:46][C:47](=[O:48])[CH3:49].[Cl:1][c:2]1[cH:3][c:4]([C:5]([O:7][c:6]2[cH:8][cH:9][cH:10][c:11]([CH3:12])[cH:13]2)=[O:14])[cH:15][cH:16][n:17]1.[ClH:43].[K+:38].[K+:39].[O:40]=[C:41]=[O:42].[OH2:50].[c:18]1(-[c:28]2[cH:29][cH:30][cH:31][cH:32][cH:33]2)[c:19]([S:24](=[O:25])(=[O:26])[NH2:27])[cH:20][cH:21][cH:22][cH:23]1>>[Cl:1][c:2]1[cH:3][c:4]([C:5](=[O:7])[NH:27][S:24]([c:19]2[c:18](-[c:28]3[cH:29][cH:30][cH:31][cH:32][cH:33]3)[cH:23][cH:22][cH:21][cH:20]2)(=[O:25])=[O:26])[cH:15][cH:16][n:17]1

Participants

9

Reactant 8

HCID 280Carbon DioxideHCID 313Hydrochloric AcidHCID 813Potassium Cation2×HCID 962WaterHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 123715202-Phenylbenzene-1-sulfonamideHCID 20187520HCID 20187520, compound

Product 1

HCID 13924302HCID 13924302, compound

Sources & evidence

ORD record
ord-5ced1bc4eb874f9797f5ca9db3c6d481
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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