Dimethyl Sulfoxide → HCID 18459339, compound

HRID 179905Notes

Reaction equation

HRID 179905 reaction equation
[C:47](=[O:48])([O-:49])[O-:50].[C:53](=[O:54])([O-:55])[OH:56].[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][C:9](=[O:10])[c:11]1[cH:12][cH:13][c:14]([O:15][c:16]2[n:17][c:18]([F:25])[c:19]([F:24])[c:20]([F:23])[c:21]2[F:22])[cH:26][cH:27]1.[CH3:58][S:59](=[O:60])[CH3:61].[K+:46].[K+:51].[K+:52].[K+:57].[N+:28](=[O:29])([O-:30])[c:31]1[c:32]([O:38][CH2:39][c:40]2[cH:41][cH:42][cH:43][cH:44][cH:45]2)[cH:33][c:34]([O-:35])[cH:36][cH:37]1>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][C:9](=[O:10])[c:11]1[cH:12][cH:13][c:14]([O:15][c:16]2[n:17][c:18]([F:25])[c:19]([F:24])[c:20]([O:35][c:34]3[cH:33][c:32]([O:38][CH2:39][c:40]4[cH:41][cH:42][cH:43][cH:44][cH:45]4)[c:31]([N+:28](=[O:29])[O-:30])[cH:37][cH:36]3)[c:21]2[F:22])[cH:26][cH:27]1

Participants

7

Reactant 6

HCID 679Dimethyl SulfoxideHCID 769Bicarbonate IonHCID 813Potassium Cation4×HCID 19660Carbonate IonHCID 184593372-(4-Benzyloxycarbonylphenoxy)-3,4,5,6-tetrafluoropyridineHCID 178526698HCID 178526698, compound

Product 1

HCID 18459339HCID 18459339, compound

Sources & evidence

ORD record
ord-7019086ca1434bd8bb6cb27c54565180
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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