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Thionyl Chloride → 3-Nitro-5-(trifluoromethyl)benzoyl chloride

HRID 446254
Notes
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Reaction equation

HRID 446254 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:12]=1)[C:7](O)=[O:8])([O-:3])=[O:2].S(Cl)([Cl:19])=O>>[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:12]=1)[C:7]([Cl:19])=[O:8])([O-:3])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24386Thionyl ChlorideHCID 6166023-Nitro-5-(trifluoromethyl)benzoic acid

Product 1

HCID 226083993-Nitro-5-(trifluoromethyl)benzoyl chloride

Procedure

A solution of thionyl chloride (30 ml) and 3-nitro-5-(trifluoromethyl)benzoic acid (10 g) was heated to reflux for 2 h. The reaction mixture was concentrated under reduced pressure and treated with toluene (10 ml) which was then removed under reduced pressure to afford 3-nitro-5-(trifluoromethyl)benzoyl chloride.

Workup

  1. temperatureto reflux for 2 h
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additiontreated with toluene (10 ml) which
  4. customwas then removed under reduced pressure

Sources & evidence

ORD record
ord-d15a3f09a9ea4dde9675ae84279fc827
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08476434B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes