Phosphorus tribromide → 1-Bromo-2-bromomethyl-5-fluoro-4-methoxy-benzene

HRID 2038735Notes

Reaction equation

HRID 2038735 reaction equation
P(Br)(Br)[Br:2].[Br:5][C:6]1[CH:11]=[C:10]([F:12])[C:9]([O:13][CH3:14])=[CH:8][C:7]=1[CH2:15]O>C(Cl)Cl>[Br:5][C:6]1[CH:11]=[C:10]([F:12])[C:9]([O:13][CH3:14])=[CH:8][C:7]=1[CH2:15][Br:2]

Participants

4

Procedure

Phosphorus tribromide (11.56 mL, 122.5 mmol) was added to a solution of (2-bromo-4-fluoro-5-methoxy-phenyl)-methanol (Preparation 33, 14.4 g, 61.26 mmol) in DCM (235 mL) at 0° C. The reaction was allowed to warm to room temperature and stirred at that temperature for 18 hours. The reaction mixture was cooled to 0° C. and quenched by slow addition of saturated sodium hydrogen carbonate aqueous solution until effervescence had ceased. The layers were separated and the aqueous layer was extracted with DCM (2×100 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo to give the title compound as a white solid (17.48 g) in a 96% yield.

Workup

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. customquenched by slow addition of saturated sodium hydrogen carbonate aqueous solution until effervescence
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted with DCM (2×100 mL)
  5. dry with materialThe combined organic layers were dried over MgSO4
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-84158d82b1794552a47f6341b2e0f892
Source dataset
uspto-grants-2013_11
Patent number
US08575336B2

Reaction notes

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