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Tetrahydrofuran → 5-Methylsulfonyltetrazole

HRID 1942324
ノート
印刷プレビュー

反応式

HRID 1942324 の反応式
CS[C:3]1[NH:7][N:6]=[N:5][N:4]=1.[S:8]([O-:13])(O[O-])(=O)=[O:9].[K+].[K+].[CH2:16]1COCC1>O>[CH3:16][S:8]([C:3]1[NH:7][N:6]=[N:5][N:4]=1)(=[O:13])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8028TetrahydrofuranHCID 10313463Potassium peroxymonosulphateHCID 178503621HCID 178503621、化合物

生成物 1

HCID 1785048625-Methylsulfonyltetrazole

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a stirred solution of 5-(methylthio)-1H-tetrazole (300 mg; Aldrich Chemical Company, Inc., Milwaukee, Wis.) in THF (15 mL) and water (15 mL) was added potassium peroxomonosulfate (Oxone®, DuPont Specialty Chemicals, Deepwater, N.J., USA) (3.18 g). After stirring at room temperature for five days, the reaction mixture was filtered and the filtercake was washed with THF. The filtrate was concentrated under reduced pressure. Crude NMR showed this to be a mixture of desired product and starting material, so the mixture was taken up in methanol and treated with potassium peroxomonosulfate (Oxone®, DuPont Specialty Chemicals, Deepwater, N.J., USA). After stirring at room temperature for five days, the reaction mixture was filtered and the filtercake was washed with methanol. The filtrate was concentrated under reduced pressure to afford 0.400 g of impure (I-11a)as a solid which was used in the next step without purification; m/z 146.9 (M−H)−.

後処理

  1. filtrationthe reaction mixture was filtered
  2. washthe filtercake was washed with THF
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. additiona mixture of desired product
  5. additiontreated with potassium peroxomonosulfate (Oxone®, DuPont Specialty Chemicals, Deepwater, N.J., USA)
  6. stirringAfter stirring at room temperature for five days
  7. filtrationthe reaction mixture was filtered
  8. washthe filtercake was washed with methanol
  9. concentrationThe filtrate was concentrated under reduced pressure
  10. customto afford 0.400 g of impure
  11. customa solid which was used in the next step without purification

出典と根拠

ORDレコード
ord-9f26e387237440c6ba49cf9e61937f0c
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08389552B2

反応ノート

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