Methanol → 2-Propenoic acid, 3-(2-fluorophenyl)-, methyl ester

HRID 2257831Notes

Reaction equation

HRID 2257831 reaction equation
[F:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[CH:4]=[CH:5][C:6]([OH:8])=[O:7].[CH3:13]O.S(Cl)(Cl)=O>C(Cl)(Cl)Cl>[F:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[CH:4]=[CH:5][C:6]([O:8][CH3:13])=[O:7]

Participants

5

Conditions

Temperature
0 °C

Procedure

15 gm of 2-fluorocinnamic acid was suspended into 100 ml of methanol. While maintaining the suspension at 0° C., 1.7 gm of thionyl chloride was added slowly. After the addition, the mixture was stirred for 30 minutes at 0° C. and for 4 hour at room temperature. The residue obtained by the removal of the solvent was subjected to silica gel column chromatography using chloroform as an eluant to obtain fractions containing the target compound. The fractions were concentrated to produce 17.8 gm of the title compound.

Workup

  1. additionAfter the addition
  2. customThe residue obtained by the removal of the solvent
  3. customto obtain fractions
  4. additioncontaining the target compound
  5. concentrationThe fractions were concentrated

Sources & evidence

ORD record
ord-ac9dae46fc2d4d87b28af45ff7fc268a
Source dataset
uspto-grants-1997_08
Patent number
US05658920

Reaction notes

Loading…