Methanol → Methyl (4-chloro-3-fluorophenyl)acetate

HRID 2078280Notes

Reaction equation

HRID 2078280 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:4][C:3]=1[F:12].OS(O)(=O)=O.[CH3:18]O>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH3:18])=[O:10])=[CH:4][C:3]=1[F:12]

Participants

4

Procedure

A solution of 2-(4-chloro-3-fluorophenyl)acetic acid (10.07 g, 53.4 mmol) and concentrated H2SO4 (0.297 mL, 5.34 mmol) in MeOH (200 mL, 4940 mmol) was stirred at 95° C. for 17 hours in a 350 mL sealed vessel. The solution was concentrated in vacuo and then made basic with 1N NaOH(aq) (100 mL). The resulting mixture was extracted with EtOAc (2×100 mL), washed with water (100 mL), and then washed with brine (75 mL). The combined organic layers were dried over MgSO4, concentrated, and dried in vacuo to give methyl 2-(4-chloro-3-fluorophenyl)acetate (10.80 g). MS m/e=203.2 (M+H)+.

Workup

  1. customsealed vessel
  2. concentrationThe solution was concentrated in vacuo
  3. extractionThe resulting mixture was extracted with EtOAc (2×100 mL)
  4. washwashed with water (100 mL)
  5. washwashed with brine (75 mL)
  6. dry with materialThe combined organic layers were dried over MgSO4
  7. concentrationconcentrated
  8. customdried in vacuo

Sources & evidence

ORD record
ord-46e9ec6affe849f19f805f4bb1ef8b2d
Source dataset
uspto-grants-2011_04
Patent number
US07928139B2

Reaction notes

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