alpha-Bromo-o-chlorotoluene → HCID 86602108, compound

HRID 899246Notes

Reaction equation

HRID 899246 reaction equation
[CH2:1]([O:3][C:4](=[O:14])[CH2:5][P:6]([O:11][CH2:12][CH3:13])([O:8][CH2:9][CH3:10])=[O:7])[CH3:2].[H-].[Na+].Br[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[Cl:25]>CN(C)C=O>[Cl:25][C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=1[CH2:18][CH:5]([P:6]([O:8][CH2:9][CH3:10])([O:11][CH2:12][CH3:13])=[O:7])[C:4]([O:3][CH2:1][CH3:2])=[O:14]

Participants

5

Procedure

To a stirred solution of ethyl(diethoxyphosphoryl)acetate (10.0 g, 44.6 mmol) in N,N-dimethylformamide (100 mL) was added 60% sodium hydride in mineral oil (1.96 g, 49.1 mmol) at 0° C. and the mixture was stirred for 1 h at the same temperature. To the mixture was added 1-(bromomethyl)-2-chlorobenzene (6.35 mL, 49.1 mmol) at 0° C. and the resulting mixture was stirred for 18 h at the room temperature. The reaction mixture was quenched by the addition of water, then extracted with diethyl ether (200 mL×2), and the combined organic layers were washed with water (100 mL) and brine (100 mL), dried over sodium sulfate, and evaporated. The residue was purified by column chromatography on silica gel (500 g) eluting with hexane/ethyl acetate (1/1) to afford 14.6 g (93%) of the title compound as a colorless oil:

Workup

  1. stirringthe resulting mixture was stirred for 18 h at the room temperature
  2. customThe reaction mixture was quenched by the addition of water
  3. extractionextracted with diethyl ether (200 mL×2)
  4. washthe combined organic layers were washed with water (100 mL) and brine (100 mL)
  5. dry with materialdried over sodium sulfate
  6. customevaporated
  7. customThe residue was purified by column chromatography on silica gel (500 g)
  8. washeluting with hexane/ethyl acetate (1/1)

Sources & evidence

ORD record
ord-c7a289d2361f45cf9186abf1c344802b
Source dataset
uspto-grants-2008_04
Patent number
US07354925B2

Reaction notes

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