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Thionyl Chloride → (4'-Chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetyl chloride

HRID 922114
Notes
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Reaction equation

HRID 922114 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[C:10]([CH2:15][C:16](O)=[O:17])[CH:9]=2)=[CH:4][C:3]=1[F:19].S(Cl)([Cl:22])=O>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[C:10]([CH2:15][C:16]([Cl:22])=[O:17])[CH:9]=2)=[CH:4][C:3]=1[F:19]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24386Thionyl ChlorideHCID 67375533(4'-Chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetic acid

Product 1

HCID 86676714(4'-Chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetyl chloride

Conditions

Temperature
80 °C

Procedure

10.00 g (35.88 mmol) of (4′-chloro-3′-fluoro-4-methylbiphenyl-3-yl)acetic acid (Example 1A) were dissolved in 24.33 g (204.51 mmol) of thionyl chloride. The reaction mixture was stirred at 80° C. for one hour and then concentrated under reduced pressure. Drying under fine vacuum gave 10.54 g (99% of theory) of the title compound as a brownish oil.

Workup

  1. concentration
concentrated under reduced pressure
  • customDrying under fine vacuum
  • Sources & evidence

    ORD record
    ord-31d95c05899e4440813f3acae9735a28
    Source dataset
    uspto-grants-2016_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09278925B2

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes