tert-Butyl 2-bromo-2-methylpropionate → HCID 11201387, compound

HRID 1945203Notes

Reaction equation

HRID 1945203 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([S:9][C:10]2[CH:15]=[CH:14][C:13]([S:16]([CH3:19])(=[O:18])=[O:17])=[CH:12][C:11]=2[Cl:20])[CH:3]=1.C([O:25][C:26](=[O:31])[C:27](Br)([CH3:29])[CH3:28])(C)(C)C>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:27]([CH3:29])([CH3:28])[C:26]([OH:31])=[O:25])=[C:4]([S:9][C:10]2[CH:15]=[CH:14][C:13]([S:16]([CH3:19])(=[O:18])=[O:17])=[CH:12][C:11]=2[Cl:20])[CH:3]=1

Participants

3

Reactant 2

HCID 90290tert-Butyl 2-bromo-2-methylpropionateHCID 669956224-Chloro-2-[[2-chloro-4-(methylsulfonyl)phenyl]thio]phenol

Product 1

HCID 11201387HCID 11201387, compound

Procedure

The title compound was prepared by the method of example 1 step (iv) using the product from example 7 step (iii) and tert-butyl-2-bromoisobutyrate, yield 0.028 g.

Sources & evidence

ORD record
ord-3243587a3169430caf8cffa955823155
Source dataset
uspto-grants-2013_03
Patent number
US08394986B2

Reaction notes

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