Chloride → t-Butyl 3-acetoxy-5-methyl-4-nitrophenylacetate
Reaction equation
[C:1]([CH3:2])(=[O:3])[O:4][c:5]1[cH:6][c:7]([CH2:14][C:15](=[O:16])[O:17][C:18]([CH3:19])([CH3:20])[CH3:21])[cH:8][cH:9][c:10]1[N+:11](=[O:12])[O-:13].[CH3:23][Mg+:24].[CH3:44][CH2:45][O:46][CH2:47][CH3:48].[Cl-:22].[Cl:25][C:26]1=[C:37]([Cl:38])[C:35](=[O:36])[C:32]([C:33]#[N:34])=[C:29]([C:30]#[N:31])[C:27]1=[O:28].[O:39]1[CH2:40][CH2:41][CH2:42][CH2:43]1>>[C:1]([CH3:2])(=[O:3])[O:4][c:5]1[cH:6][c:7]([CH2:14][C:15](=[O:16])[O:17][C:18]([CH3:19])([CH3:20])[CH3:21])[cH:8][c:9]([CH3:26])[c:10]1[N+:11](=[O:12])[O-:13]Participants
7
Sources & evidence
- ORD record
- ord-be3c947278e745e09dd408832d3c3b62
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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