Thionyl Chloride → 3-Fluoro-4-nitrobenzoyl chloride

HRID 73650

Reaction equation

HRID 73650 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12])[C:5](O)=[O:6].O=S(Cl)[Cl:16]>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12])[C:5]([Cl:16])=[O:6]

Participants

4

Conditions

Temperature
110 °C

Procedure

To a suspension of 3-fluoro-4-nitrobenzoic acid (30 g, 162.0 mmol) in toluene (500 mL) was added SOCl2 (35 mL, 486 mmol). The reaction was heated to 110° C. at which point the reaction became homogeneous. The reaction was stirred at 110° C. for 3 h. The reaction had not gone to completion so an additional portion of SOCl2 (10 mL) was added. The reaction was stirred for an additional 3 h. A small amount of starting material remained thus a final portion of SOCl2 (10 mL) was added and the reaction was heated for 2 h. The resulting green solution was cooled to room temperature and allowed to stand over night. The reaction mixture was filtered and concentrated in vacuo. Toluene (300 mL) was added to the resulting oil and removed under reduced pressure (2×). The product was used without further purification.

Workup

  1. additionwas added
  2. stirringThe reaction was stirred for an additional 3 h
  3. additionwas added
  4. temperaturethe reaction was heated for 2 h
  5. temperatureThe resulting green solution was cooled to room temperature
  6. waitto stand over night
  7. filtrationThe reaction mixture was filtered
  8. concentrationconcentrated in vacuo
  9. additionToluene (300 mL) was added to the resulting oil
  10. customremoved under reduced pressure (2×)
  11. customThe product was used without further purification

Sources & evidence

ORD record
ord-26b142a55cd34d9abce426500980b247
Source dataset
uspto-grants-2014_09
Patent number
US08829185B2

Linked notes

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