Potassium Cation → HCID 178495400, compound

HRID 187393Notes

Reaction equation

HRID 187393 reaction equation
[C:31](=[O:32])([O-:33])[O-:34].[CH3:37][C:38]#[N:39].[F:17][c:18]1[cH:19][c:20]2[c:21]([cH:29][cH:30]1)[S:22](=[O:27])(=[O:28])[CH2:23][CH2:24][CH2:25][O:26]2.[K+:35].[K+:36].[OH:1][c:2]1[cH:3][c:4]([C:5](=[O:6])[OH:7])[cH:8][c:9]([O:11][CH:12]([CH2:13][O:14][CH3:15])[CH3:16])[cH:10]1>>[O:1]([c:2]1[cH:3][c:4]([C:5](=[O:6])[OH:7])[cH:8][c:9]([O:11][CH:12]([CH2:13][O:14][CH3:15])[CH3:16])[cH:10]1)[c:18]1[cH:19][c:20]2[c:21]([cH:29][cH:30]1)[S:22](=[O:27])(=[O:28])[CH2:23][CH2:24][CH2:25][O:26]2

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6342AcetonitrileHCID 19660Carbonate IonHCID 576632198-fluoro-3,4-dihydro-2H-1,5-benzoxathiepine 5,5-dioxideHCID 674851293-Hydroxy-5-(1-methoxypropan-2-yloxy)benzoic acid

Product 1

HCID 178495400HCID 178495400, compound

Sources & evidence

ORD record
ord-89a1d6697a244b6b92ddcc7bb134ccee
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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