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Methyl iodide → HCID 22101417, compound

HRID 1457947
Notes
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Reaction equation

HRID 1457947 reaction equation
[Br:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([S:12]([CH3:15])(=[O:14])=[O:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].CI.[C:18](=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[Br:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([S:12]([CH3:15])(=[O:14])=[O:13])=[CH:7][C:3]=1[C:4]([O:6][CH3:18])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 221013972-Bromo-4-fluoro-5-methylsulphonylbenzoic acid

Product 1

HCID 22101417HCID 22101417, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

5.8 g of 2-bromo-4-fluoro-5-methylsulphonylbenzoic acid are stirred, at room temperature for 12 h, in 20 ml of DMF together with 3.7 ml of methyl iodide and 8.3 g of potassium carbonate. The reaction mixture is then concentrated and 50 ml of water are added to it. The resulting precipitate is filtered off with suction and dried. Methyl 2-bromo-4-fluoro-5-methylsulphonylbenzoate is obtained, m.p. 126°.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. concentrationThe reaction mixture is then concentrated
  2. addition50 ml of water are added to it
  3. filtrationThe resulting precipitate is filtered off with suction
  4. customdried

Sources & evidence

ORD record
ord-e7e81265df5449dca25d05449d7eb82e
Source dataset
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05849796

Reaction notes

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