Acetic Anhydride → HCID 70601480, compound

HRID 1447985Notes

Reaction equation

HRID 1447985 reaction equation
[CH3:1][S:2]([CH2:4][C:5]1[O:6][C:7]2[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9](=[O:11])[CH:10]=1)=O.[C:16]([O:19]C(=O)C)(=[O:18])[CH3:17]>>[C:16]([OH:19])(=[O:18])[CH3:17].[CH3:1][S:2][CH:4]([OH:18])[C:5]1[O:6][C:7]2[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9](=[O:11])[CH:10]=1

Participants

3

Reactant 2

HCID 7918Acetic AnhydrideHCID 124017022-[(Methylsulfinyl)methyl]-4H-1-benzopyran-4-one

Product 1

HCID 70601480HCID 70601480, compoundYield 90%

Procedure

A solution of 2-[(methylsulfinyl)methyl]-4H-1-benzopyran-4-one (2.22 g, 0.01 m) in acetic anhydride (15 ml) was refluxed under nitrogen for 5 hours. The solvent was removed under reduced pressure to give a brown gum, which crystallized on standing. Recrystallization from methanol gave off-white crystals (2.36 g, 90%), m.p. 123°-125°.

Workup

  1. customThe solvent was removed under reduced pressure
  2. customto give a brown gum, which
  3. customcrystallized
  4. customRecrystallization from methanol

Sources & evidence

ORD record
ord-c455ffaa086644969b94760d6b74e789
Source dataset
uspto-grants-1979_12
Patent number
US04179447

Reaction notes

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