Methanol → Methyl 4-bromo-2-chloro-5-fluorobenzoate
Reaction equation
[Br:1][C:2]1[C:10]([F:11])=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([Cl:12])[CH:3]=1.O=S(Cl)Cl.[CH3:17]O>>[Br:1][C:2]1[C:10]([F:11])=[CH:9][C:5]([C:6]([O:8][CH3:17])=[O:7])=[C:4]([Cl:12])[CH:3]=1Participants
4
Conditions
- Temperature
- 0 °C
Procedure
4-bromo-2-chloro-5-fluorobenzoic acid (Apollo PC9723, 5 g; 19.73 mmol; 1 eq.) was dissolved in MeOH (100 mL). The solution was cooled down to 0° C. SOCl2 (4.29 mL; 59.18 mmol; 3 eq.) was added dropwise (addition took 15 min and IT increased to 9° C.). The reaction mixture was stirred at RT for 3 days. The reaction mixture was concentrated and the crude mixture was dissolved in EtOAc (200 mL) and washed with a saturated aqueous solution of NaHCO3(50 mL), brine (50 mL), dried over MgSO4 and concentrated affording the title compound as a white solid (5.04 g, 95%). 1H NMR (DMSO-d6, 300 MHz) δ 8.10-8.08 (d, J=6.30 Hz), 1H), 7.86-7.83 (d, J=8.82 Hz, 1H), 3.87 (s, 3H). HPLC (Method A) Rt 4.32 min (Purity: 99.7%).
Workup
- addition(addition took 15 min and IT increased to 9° C.)
- concentrationThe reaction mixture was concentrated
- dissolutionthe crude mixture was dissolved in EtOAc (200 mL)
- washwashed with a saturated aqueous solution of NaHCO3(50 mL), brine (50 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-5cf91f241bed44d7926c6cd74dcaf865
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08202865B2
Reaction notes
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