Acetone → HCID 14349145, compound

HRID 86962Notes

Reaction equation

HRID 86962 reaction equation
[C:35](=[O:36])([O-:37])[O-:38].[CH2:13]([c:14]1[cH:15][cH:16][cH:17][cH:18][cH:19]1)[O:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH:26]([OH:27])[c:28]1[cH:29][c:30]([OH:34])[cH:31][cH:32][cH:33]1.[CH3:43][C:44](=[O:45])[CH3:46].[Cl:1][CH2:2][c:3]1[n:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]2[cH:11][cH:12]1.[I-:42].[K+:39].[K+:40].[K+:41]>>[CH2:2]([c:3]1[n:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]2[cH:11][cH:12]1)[O:34][c:30]1[cH:29][c:28]([CH:26]([CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][O:20][CH2:13][c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)[OH:27])[cH:33][cH:32][cH:31]1

Participants

7

Reactant 6

HCID 180AcetoneHCID 813Potassium Cation3×HCID 19660Carbonate IonHCID 203942-(Chloromethyl)quinolineHCID 30165Iodide IonHCID 21280520HCID 21280520, compound

Product 1

HCID 14349145HCID 14349145, compound

Sources & evidence

ORD record
ord-11893b2a3bde41488d86df28352dbf4a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

Loading…