Pyridine → 2-Methylsulfinyl-5-(1H-tetrazol-1-yl)benzoic Acid

HRID 2230589Notes

Reaction equation

HRID 2230589 reaction equation
[CH3:1][S:2][C:3]1[CH:11]=[CH:10][C:9]([N:12]2[CH:16]=[N:15][N:14]=[N:13]2)=[CH:8][C:4]=1[C:5]([OH:7])=[O:6].N1C=CC=CC=1.[Br-].[Br-].[Br-].C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.S(=O)(O)[O-:57].[Na+]>O.O1CCCC1>[CH3:1][S:2]([C:3]1[CH:11]=[CH:10][C:9]([N:12]2[CH:16]=[N:15][N:14]=[N:13]2)=[CH:8][C:4]=1[C:5]([OH:7])=[O:6])=[O:57]

Participants

7

Reactant 4

HCID 1049PyridineHCID 17977687Phenyltrimethylammonium bromide dibromideHCID 184645182-Methylthio-5-(1H-tetrazol-1-yl)benzoic AcidHCID 23665763Sodium Bisulfite

Product 1

HCID 184645052-Methylsulfinyl-5-(1H-tetrazol-1-yl)benzoic Acid

Reagents, catalysts & solvents 2

HCID 962WaterSolvent2×HCID 8028TetrahydrofuranSolvent

Procedure

Combine 2-methylthio-5-(1H-tetrazol-1-yl)benzoic acid (0.50 g, 2.0 mmol), pyridine (20 mL) and water (20 mL). Cool in an ice bath. Add phenyltrimethylammonium tribromide (0.75 g, 2 mmol) and tetrahydrofuran (20 mL). Warm to ambient temperature. After 1 hour, add a solution a of sodium bisulfite (1 g) in water (1 mL). Extract the reaction mixture with ethyl acetate and then dichloromethane. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give a residue. the title compound. Chromatograph the residue on silica gel eluting sequentially with ethyl acetate and then 10% methanol/ethyl acetate to give methyl 2-methylsulfinyl-5-(1H-tetrazol-1-yl)benzoate.

Workup

  1. temperatureCool in an ice bath
  2. extractionExtract the reaction mixture with ethyl acetate
  3. dry with materialdry over MgSO4
  4. filtrationfilter
  5. customevaporate in vacuo
  6. customto give a residue

Sources & evidence

ORD record
ord-dc1b5f50eb82427ca69980233f37a3bc
Source dataset
uspto-grants-2002_07
Patent number
US06423704B1

Reaction notes

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