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Dimethyl Sulfoxide → HCID 53666760, compound

HRID 2125199
Notes
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Reaction equation

HRID 2125199 reaction equation
[C:13](=[O:14])([O-:15])[O-:16].[CH2:32]([CH2:33][O:34][CH3:35])[O:36][CH3:37].[CH3:38][S:39](=[O:40])[CH3:41].[F:19][c:20]1[c:21]([F:31])[c:22]([F:30])[c:23]([C:24]([F:25])([F:26])[Br:27])[cH:28][cH:29]1.[K+:17].[K+:18].[OH:1][N:2]1[C:3](=[O:12])[c:4]2[c:5]([cH:8][cH:9][cH:10][cH:11]2)[C:6]1=[O:7]>>[O:1]([N:2]1[C:3](=[O:12])[c:4]2[c:5]([cH:8][cH:9][cH:10][cH:11]2)[C:6]1=[O:7])[C:24]([c:23]1[c:22]([F:30])[c:21]([F:31])[c:20]([F:19])[cH:29][cH:28]1)([F:25])[F:26]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 80711,2-DimethoxyethaneHCID 10665N-HydroxyphthalimideHCID 19660Carbonate IonHCID 223810251-[Bromo(difluoro)methyl]-2,3,4-trifluorobenzene

Product 1

HCID 53666760HCID 53666760, compound

Sources & evidence

ORD record
ord-fc83f9a574234356b91f9be2bcc57537
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes