Dimethyl Sulfoxide → HCID 135725108, compound

HRID 2156447Notes

Reaction equation

HRID 2156447 reaction equation
[C:33](=[O:34])([O-:35])[O-:36].[C:4]([CH3:5])([CH3:6])([CH3:7])[c:8]1[cH:9][c:10](-[c:19]2[o:20][cH:21][c:22]([CH2:24][CH2:25][I:26])[n:23]2)[cH:11][c:12]([C:15]([CH3:16])([CH3:17])[CH3:18])[c:13]1[OH:14].[CH3:27][CH2:28][O:29][C:30](=[O:31])[CH3:32].[CH3:39][S:40]([CH3:41])=[O:42].[CH3:43][CH2:44][CH2:45][CH2:46][CH2:47][CH3:48].[K+:37].[K+:38].[Na:1][C:2]#[N:3]>>[C:2](#[N:3])[CH2:25][CH2:24][c:22]1[cH:21][o:20][c:19](-[c:10]2[cH:9][c:8]([C:4]([CH3:5])([CH3:6])[CH3:7])[c:13]([OH:14])[c:12]([C:15]([CH3:16])([CH3:17])[CH3:18])[cH:11]2)[n:23]1

Participants

8

Reactant 7

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 8058HexaneHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 135725039HCID 135725039, compoundHCID 178511850HCID 178511850, compound

Product 1

HCID 135725108HCID 135725108, compound

Sources & evidence

ORD record
ord-e90e5acc5c80402881ecfe404f768666
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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