Ethyl bromoacetate → HCID 12898550, compound

HRID 2050063Notes

Reaction equation

HRID 2050063 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH:8]([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10])[CH:5]=[C:4]([CH3:17])[C:3]=1[OH:18].Br[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22].C(=O)([O-])[O-:27].[K+].[K+]>C(#N)C>[F:16][C:13]([F:14])([F:15])[C:8]([C:6]1[CH:7]=[C:2]([CH3:1])[C:3]([O:18][CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:4]([CH3:17])[CH:5]=1)([OH:27])[C:9]([F:10])([F:11])[F:12]

Participants

5

Procedure

To 2,6-dimethyl-4-(hexafluoro-2-propyl)phenol [Farah, et al, J. Org. Chem., 30, 1003 (1965)], (10.0 g=35 mmol) in 100 ml acetonitrile add ethyl bromoacetate (6.9 g=42 mmol) and potassium carbonate (9.7 g=69 mmol). Stir 5 hours, filter and concentrate. Partition between ether and 1.0 N HCl. Dry and concentrate the ether extract. Recrystallize from ether-hexane to obtain, as white crystals, m.p. 99°-101° C., ethyl 2-[4-(hexafluoro-2-hydroxy-2-propyl)-2,6-dimethylphenoxy]acetate.

Workup

  1. filtrationfilter
  2. concentrationconcentrate
  3. customPartition between ether and 1.0 N HCl
  4. customDry
  5. concentrationconcentrate the ether
  6. extractionextract
  7. customRecrystallize from ether-hexane

Sources & evidence

ORD record
ord-75e718b80742459797763ee856c78210
Source dataset
uspto-grants-1980_04
Patent number
US04199597

Reaction notes

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