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Potassium Cation → 2-(4-Bromo-phenyl)-4-(tert-butyl-dimethyl-silanyloxy)-butyric acid ethyl ester

HRID 182967
Notes
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Reaction equation

HRID 182967 reaction equation
[Br:1][CH2:2][CH2:3][O:4][Si:5]([CH3:6])([CH3:7])[C:8]([CH3:9])([CH3:10])[CH3:11].[CH2:12]([CH3:13])[O:14][C:15]([CH2:16][c:17]1[cH:18][cH:19][c:20]([Br:23])[cH:21][cH:22]1)=[O:24].[CH3:25][C:26]([CH3:27])([O-:28])[CH3:29].[CH3:31][N:32]([CH3:33])[CH:34]=[O:35].[K+:30]>>[CH2:2]([CH2:3][O:4][Si:5]([CH3:6])([CH3:7])[C:8]([CH3:9])([CH3:10])[CH3:11])[CH:16]([C:15]([O:14][CH2:12][CH3:13])=[O:24])[c:17]1[cH:18][cH:19][c:20]([Br:23])[cH:21][cH:22]1
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 813Potassium CationHCID 6228DimethylformamideHCID 3608067(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 45749132-Methylpropan-2-olateHCID 7020609Ethyl 2-(4-bromophenyl)acetate

Product 1

HCID 592383032-(4-Bromo-phenyl)-4-(tert-butyl-dimethyl-silanyloxy)-butyric acid ethyl ester

Sources & evidence

ORD record
ord-64bde28621484285a95e63d709d96262
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes