2-Bromophenol → HCID 69417921, compound

HRID 1373639Notes

Reaction equation

HRID 1373639 reaction equation
[CH3:1][O:2][C:3](=[O:13])[C:4]([CH3:12])([CH3:11])[CH2:5][O:6]S(C)(=O)=O.[Br:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1O.C([O-])([O-])=O.[Cs+].[Cs+]>C(#N)C>[CH3:1][O:2][C:3](=[O:13])[C:4]([CH3:12])([CH3:11])[CH2:5][O:6][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[Br:14]

Participants

5

Conditions

Temperature
100 °C

Procedure

A first intermediate compound 3-(2-Bromo-phenoxy)-2,2-dimethyl-propionic acid, was produced as follows: To a mixture of 3-methanesulfonyloxy-2,2-dimethyl-propionic acid methyl ester (20.00 g, 95.23 mmol) and 2-bromophenol (16.48 g, 95.23 mmol) in acetonitrile (200 mL) was added Cs2CO3 (46.50 g, 142.80 mmol) and the mixture was heated at 100° C. in a sealed flask overnight. The resulting suspension was filtered. The solvent was evaporated and the crude material was partitioned between dichloromethane (100 mL) and water (100 mL). The organic layer was separated and the aqueous layer was extracted with dichloromethane (50 mL), dried over Na2SO4 and evaporation of the solvent gave 3-(2-bromo-phenoxy)-2,2-dimethyl-propionic acid methyl ester (19.00 g, 70%) as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 7.55 (d, 1H), 7.26–7.22 (m, 1H), 6.87–6.80 (m, 2H), 4.02 (s, 2H), 3.72 (s, 3H), 1.40 (s, 6H).

Workup

  1. filtrationThe resulting suspension was filtered
  2. customThe solvent was evaporated
  3. customthe crude material was partitioned between dichloromethane (100 mL) and water (100 mL)
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted with dichloromethane (50 mL)
  6. dry with materialdried over Na2SO4 and evaporation of the solvent

Sources & evidence

ORD record
ord-13f5cca6f640490b9743dd2d46b7bb3d
Source dataset
uspto-grants-2007_01
Patent number
US07160888B2

Reaction notes

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