Oxalyl chloride → HCID 23445624, compound
Reaction equation
[CH2:1]([CH3:2])[c:3]1[cH:4][c:5]([C:6](=[O:7])[OH:8])[cH:9][c:10]([CH2:14][CH3:15])[c:11]1[O:12][CH3:13].[CH2:23]([c:24]1[cH:25][cH:26][cH:27][cH:28][cH:29]1)[c:30]1[o:31][c:32]([CH3:36])[c:33]([CH3:35])[cH:34]1.[Cl:16][C:17]([C:18]([Cl:19])=[O:20])=[O:21].[Sn:22]>>[CH2:1]([CH3:2])[c:3]1[cH:4][c:5]([C:6](=[O:8])[c:34]2[c:30]([CH2:23][c:24]3[cH:25][cH:26][cH:27][cH:28][cH:29]3)[o:31][c:32]([CH3:36])[c:33]2[CH3:35])[cH:9][c:10]([CH2:14][CH3:15])[c:11]1[O:12][CH3:13]Participants
5
Sources & evidence
- ORD record
- ord-f6dbaf9551634456a8b5a52afe1ae3dc
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction notes
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