Thionyl Chloride → (4-Fluorophenoxy)acetyl chloride

HRID 1633204Notes

Reaction equation

HRID 1633204 reaction equation
[F:1][C:2]1[CH:12]=[CH:11][C:5]([O:6][CH2:7][C:8](O)=[O:9])=[CH:4][CH:3]=1.S(Cl)([Cl:15])=O>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:12]=[CH:11][C:5]([O:6][CH2:7][C:8]([Cl:15])=[O:9])=[CH:4][CH:3]=1

Participants

4

Procedure

Into a 100 ml round bottom flask equipped with a magnetic stirrer, reflux condenser equipped with a connector to a 50% sodium hydroxide trap, 6.81 g (0.040 mole) para-fluorophenoxyacetic acid (the product of Example 2), 2.96 ml (0.044 mole) thionyl chloride, and about 40 ml toluene. The reaction mixture was stirred at reflux for two hours, allowed to cool to room temperature, and then concentrated to give 7.2 g of the product, a brwon liquid.

Workup

  1. customInto a 100 ml round bottom flask equipped with a magnetic stirrer
  2. temperaturereflux condenser
  3. customequipped with a connector to a 50% sodium hydroxide trap
  4. temperatureat reflux for two hours
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-8c2280aef46a4fe7ab60c4afd38eef12
Source dataset
uspto-grants-1984_10
Patent number
US04479900

Reaction notes

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