Ethyl Bromide → 1,3-Dibromo-5-ethoxymethyl-2-methyl-benzene

HRID 1667509Notes

Reaction equation

HRID 1667509 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][OH:11])[CH:5]=[C:6]([Br:9])[C:7]=1[CH3:8].[H-].[Na+].Br[CH2:15][CH3:16]>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][O:11][CH2:15][CH3:16])[CH:5]=[C:6]([Br:9])[C:7]=1[CH3:8]

Participants

5

Conditions

Temperature
70 °C

Procedure

A mixture of (3,5-dibromo-4-methyl-phenyl)-methanol (4 g, 14.288 mmol), 60% NaH (690 mg, 28.75 mmol) and THF (72 mL) was heated to 70° C. in a sealed tube for 15 minutes. The reaction was cooled, bromoethane (3.2 mL, 42.86 mmol) was added and the reaction continued heating at 70° C. for 6 h. The reaction was cooled, poured onto water, extracted with EtOAc (×3). The organics were washed with water, brine and dried (Na2SO4). Chromatography (Hexanes/EtOAc) afforded 1,3-dibromo-5-ethoxymethyl-2-methyl-benzene (2.187 g) as a colourless oil. 1H NMR (400 MHz, d6-DMSO) δ: 1.15 (t, 3H), 2.48 (s, 3H), 3.46 (q, 2H), 4.41 (s, 2H), 7.57 (s, 2H) ppm.

Workup

  1. temperatureThe reaction was cooled
  2. temperaturethe reaction continued heating at 70° C. for 6 h
  3. temperatureThe reaction was cooled
  4. additionpoured onto water
  5. extractionextracted with EtOAc (×3)
  6. washThe organics were washed with water, brine
  7. dry with materialdried (Na2SO4)

Sources & evidence

ORD record
ord-30dc276318d84022ab8347599f6b440e
Source dataset
uspto-grants-2011_10
Patent number
US08044041B2

Reaction notes

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