Iodine → HCID 12401704, compound

HRID 1447986Notes

Reaction equation

HRID 1447986 reaction equation
[C:1](O)(=[O:3])C.CS[CH:7]([OH:19])[C:8]1[O:9][C:10]2[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=2[C:12](=[O:14])[CH:13]=1.II.[CH3:22]O>>[CH3:1][O:3][CH:7]([O:19][CH3:22])[C:8]1[O:9][C:10]2[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=2[C:12](=[O:14])[CH:13]=1

Participants

4

Reactant 3

HCID 807IodineHCID 887MethanolHCID 70601480HCID 70601480, compound

Product 1

HCID 12401704HCID 12401704, compoundYield 86%

Procedure

A stirred solution of 2-[(methylthio)hydroxymethyl)-4H-1-benzopyran-4-one acetate](2.64 g, 0.01 m) and iodine (1.39 g, 0.01 m) in methanol (50 ml) was refluxed under nitrogen for 6 hours. After cooling, the solvents were removed under reduced pressure. The red-brown oil was dissolved in chloroform and washed three times (30 ml) with aqueous saturated sodium thiosulfate. The chloroform extract was dried over sodium sulfate. Removal of the solvent under reduced pressure gave crude solid product. Recrystallization from isopropyl ether gave yellow crystals (1.9 g, 86%), m.p. 64°-68°.

Workup

  1. temperatureAfter cooling
  2. customthe solvents were removed under reduced pressure
  3. dissolutionThe red-brown oil was dissolved in chloroform
  4. washwashed three times (30 ml) with aqueous saturated sodium thiosulfate
  5. extractionThe chloroform extract
  6. dry with materialwas dried over sodium sulfate
  7. customRemoval of the solvent under reduced pressure
  8. customgave crude solid product
  9. customRecrystallization from isopropyl ether

Sources & evidence

ORD record
ord-f9cc2cf53b5c4f63a8110cdc0e2b7fb0
Source dataset
uspto-grants-1979_12
Patent number
US04179447

Reaction notes

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