Pivaloyl chloride → HCID 58372786, compound
Reaction equation
[C:63]([C:64]([CH3:65])([CH3:66])[CH3:67])(=[O:68])[Cl:69].[CH3:1][O:2][C:3]([CH2:4][c:5]1[cH:6][c:7]([O:15][c:16]2[c:17]([CH2:25][S:26][CH2:27][C:28]([F:29])([F:30])[F:31])[cH:18][c:19]([N+:22]([O-:23])=[O:24])[cH:20][cH:21]2)[c:8]([O:11][CH:12]([F:13])[F:14])[cH:9][cH:10]1)=[O:32].[CH3:33][O:34][C:35](=[O:36])[CH2:37][c:38]1[cH:39][cH:40][c:41]([O:42][CH:43]([F:44])[F:45])[c:46]([O:47][c:48]2[cH:49][cH:50][c:51]([NH2:52])[cH:53][c:54]2[CH2:55][S:56][CH2:57][C:58]([F:59])([F:60])[F:61])[cH:62]1>>[CH3:1][O:2][C:3]([CH2:4][c:5]1[cH:6][c:7]([O:15][c:16]2[c:17]([CH2:25][S:26][CH2:27][C:28]([F:29])([F:30])[F:31])[cH:18][c:19]([NH:22][C:63]([C:64]([CH3:65])([CH3:66])[CH3:67])=[O:68])[cH:20][cH:21]2)[c:8]([O:11][CH:12]([F:13])[F:14])[cH:9][cH:10]1)=[O:32]Participants
4
Sources & evidence
- ORD record
- ord-c069e9c7cf294cf19ea90a38c820e573
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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