Ethanol → Oxalic Acid

HRID 1546468Notes

Reaction equation

HRID 1546468 reaction equation
[C:25]([C:26](=[O:27])[O-:28])(=[O:29])[O-:30].[CH3:37][CH2:38][OH:39].[CH3:40][CH2:41][N:42]([CH2:43][CH3:44])[CH2:45][CH3:46].[Cl:1][c:2]1[n:3][c:4](-[n:18]2[cH:19][n:20][cH:21][cH:22]2)[c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]2[c:11]1-[c:12]1[cH:13][cH:14][cH:15][cH:16][cH:17]1.[H:23][H:24].[OH:31][C:32]([C:33](=[O:34])[OH:35])=[O:36]>>[C:25]([C:26](=[O:27])[OH:28])(=[O:29])[OH:30].[cH:2]1[n:3][c:4](-[n:18]2[cH:19][n:20][cH:21][cH:22]2)[c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]2[c:11]1-[c:12]1[cH:13][cH:14][cH:15][cH:16][cH:17]1

Participants

8

Reactant 6

HCID 702EthanolHCID 971Oxalic AcidHCID 8471TriethylamineHCID 71081OxalateHCID 1939953-Chloro-1-imidazol-1-yl-4-phenylisoquinolineHCID 178418361HCID 178418361, compound

Product 2

HCID 971Oxalic AcidHCID 21534901HCID 21534901, compound

Sources & evidence

ORD record
ord-a3875062345643b48928b8227267be18
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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