Benzoyl chloride → HCID 178460615, compound
Reaction equation
[C:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)(=[O:8])[Cl:9].[CH3:10][C:11]1([CH3:45])[C:12]2=[CH:13][CH2:14][CH:15]3[CH:16]4[CH2:17][CH2:18][CH:19]([CH:20]([CH3:21])[CH2:22][O:23][Si:24]([CH:25]([CH3:26])[CH3:27])([CH:28]([CH3:29])[CH3:30])[CH:31]([CH3:32])[CH3:33])[C:34]4([CH3:44])[CH2:35][CH2:36][CH:37]3[C:38]2([CH3:43])[CH2:39][CH2:40][CH:41]1[OH:42]>>[C:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)(=[O:8])[O:42][CH:41]1[C:11]([CH3:10])([CH3:45])[C:12]2=[CH:13][CH2:14][CH:15]3[CH:16]4[CH2:17][CH2:18][CH:19]([CH:20]([CH3:21])[CH2:22][O:23][Si:24]([CH:25]([CH3:26])[CH3:27])([CH:28]([CH3:29])[CH3:30])[CH:31]([CH3:32])[CH3:33])[C:34]4([CH3:44])[CH2:35][CH2:36][CH:37]3[C:38]2([CH3:43])[CH2:39][CH2:40]1Participants
3
Sources & evidence
- ORD record
- ord-166cf5dea2f547b2a11326eb59024329
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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