Bromide ion → HCID 178496532, compound

HRID 689899Notes

Reaction equation

HRID 689899 reaction equation
[Br-:40].[Br-:42].[C:1]([O:2][CH:5]1[CH:6]([CH:10]([CH2:11][O:12][SiH:13]([CH3:14])[CH3:15])[C:16]([CH3:17])([CH3:18])[CH3:19])[C:7](=[O:9])[NH:8]1)(=[O:3])[CH3:4].[CH3:21][O:22][CH2:23][C:24](=[S:25])[OH:26].[CH3:33][CH2:34][O:35][C:36](=[O:37])[CH3:38].[K:20].[O:27]1[CH2:28][CH2:29][O:30][CH2:31][CH2:32]1.[OH2:39].[Zn+2:41]>>[CH:5]1([S:25][C:24]([CH2:23][O:22][CH3:21])=[O:26])[CH:6]([CH:10]([CH2:11][O:12][SiH:13]([CH3:14])[CH3:15])[C:16]([CH3:17])([CH3:18])[CH3:19])[C:7](=[O:9])[NH:8]1

Participants

9

Reactant 8

HCID 259Bromide ion2×HCID 962WaterHCID 8857Ethyl AcetateHCID 312751,4-DioxaneHCID 32051Zinc(2+)HCID 5462222PotassiumHCID 173232100[3-(1-Dimethylsilyloxy-3,3-dimethylbutan-2-yl)-4-oxoazetidin-2-yl] acetateHCID 178496531HCID 178496531, compound

Product 1

HCID 178496532HCID 178496532, compound

Sources & evidence

ORD record
ord-7e01151537c44ae1bfaf2c40b762fbc0
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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