Dimethyl Sulfoxide → HCID 76671265, compound

HRID 1123599Notes

Reaction equation

HRID 1123599 reaction equation
[C:32](=[O:33])([O-:34])[O-:35].[CH3:38][S:39](=[O:40])[CH3:41].[Cl:17][c:18]1[cH:19][c:20]([OH:31])[cH:21][n:22][c:23]1[O:24][CH:25]([C:26]([F:27])([F:28])[F:29])[CH3:30].[Cl:1][c:2]1[c:3]([F:16])[cH:4][c:5]([F:15])[c:6]([C:7](=[O:8])[O:9][C:10]([CH3:11])([CH3:12])[CH3:13])[cH:14]1.[K+:36].[K+:37]>>[Cl:1][c:2]1[c:3]([O:31][c:20]2[cH:19][c:18]([Cl:17])[c:23]([O:24][CH:25]([C:26]([F:27])([F:28])[F:29])[CH3:30])[n:22][cH:21]2)[cH:4][c:5]([F:15])[c:6]([C:7](=[O:8])[O:9][C:10]([CH3:11])([CH3:12])[CH3:13])[cH:14]1

Participants

6

Reactant 5

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 19660Carbonate IonHCID 58042499tert-butyl 5-chloro-2,4-difluorobenzoateHCID 58042512HCID 58042512, compound

Product 1

HCID 76671265HCID 76671265, compound

Sources & evidence

ORD record
ord-4fbd07232cab455ab39e5888d0fefc1a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

Loading…