2-Phenoxybutanoic acid → HCID 178458321, compound
Reaction equation
[C:14]([CH3:15])([CH3:16])([CH3:17])[CH:18]1[CH:19]=[C:20]2[CH:21]=[CH:22][CH:23]([CH3:50])[C:24]([CH2:29][CH2:30][CH:31]3[CH2:32][CH:33]([C:42]([CH3:43])([CH3:44])[CH3:45])[CH:34]([O:38][SiH:39]([CH3:40])[CH3:41])[C:35](=[O:37])[O:36]3)([O:46][SiH:47]([CH3:48])[CH3:49])[CH:25]2[CH:26]([OH:28])[CH2:27]1.[O:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[CH:8]([C:9](=[O:10])[OH:11])[CH2:12][CH3:13]>>[O:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[CH:8]([C:9]([O:10][CH:26]1[CH:25]2[C:20](=[CH:19][CH:18]([C:14]([CH3:15])([CH3:16])[CH3:17])[CH2:27]1)[CH:21]=[CH:22][CH:23]([CH3:50])[C:24]2([CH2:29][CH2:30][CH:31]1[CH2:32][CH:33]([C:42]([CH3:43])([CH3:44])[CH3:45])[CH:34]([O:38][SiH:39]([CH3:40])[CH3:41])[C:35](=[O:37])[O:36]1)[O:46][SiH:47]([CH3:48])[CH3:49])=[O:11])[CH2:12][CH3:13]Participants
3
Sources & evidence
- ORD record
- ord-8add197c711c440ba6daae384e6900dd
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
Loading…