Methanol → Methyl 4-tetrahydrofuran-3-ylsulfonylbenzoate

HRID 713064Notes

Reaction equation

HRID 713064 reaction equation
[O:1]1[CH2:5][CH2:4][CH:3]([S:6][C:7]2[CH:16]=[CH:15][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:9][CH:8]=2)[CH2:2]1.[OH2:17].OOS([O-])=O.[K+].C[OH:25]>>[O:1]1[CH2:5][CH2:4][CH:3]([S:6]([C:7]2[CH:8]=[CH:9][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:15][CH:16]=2)(=[O:25])=[O:17])[CH2:2]1

Participants

5

Procedure

Methyl 4-tetrahydrofuran-3-ylsulfanylbenzoate (1.01 g, 4.24 mmol) was dissolved in methanol (25 mL), followed by the addition of water (2.5 mL), and Oxone (2.61 g, 4.24 mmol). The reaction mixture was stirred at room temperature for 24 hours. An additional 0.1 eq of Oxone (0.26 g) was added and the reaction mixture was stirred for 2 hours, then filtered and the solvent was concentrated in vacuo. The resulting residue was dissolved in dichloromethane (30 mL) and washed with water (2×25 mL). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to yield methyl 4-tetrahydrofuran-3-ylsulfonylbenzoate (1.07 g, 93%) as a yellow solid. ESI-MS m/z calc. 270.1. found 271.3 (M+1)+; Retention time: 1.02 minutes (3 min run).

Workup

  1. stirringthe reaction mixture was stirred for 2 hours
  2. filtrationfiltered
  3. concentrationthe solvent was concentrated in vacuo
  4. dissolutionThe resulting residue was dissolved in dichloromethane (30 mL)
  5. washwashed with water (2×25 mL)
  6. dry with materialThe organic layer was dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-df8f5ca20f5249fa8772575cf5abfa3e
Source dataset
uspto-grants-2015_11
Patent number
US09181273B2

Reaction notes

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