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Water → 3-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

HRID 1416320
ノート
印刷プレビュー

反応式

HRID 1416320 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:11]#[N:12])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:13][O:14][CH2:15][C:16]1OC(=O)[S:18][N:17]=1.O>CCCCCCCCCCCC>[CH3:13][O:14][CH2:15][C:16]1[N:12]=[C:11]([S:8]([C:5]2[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][CH:6]=2)(=[O:10])=[O:9])[S:18][N:17]=1
参加物反応条件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 962WaterHCID 87946p-Toluenesulphonyl cyanideHCID 218503335-Methoxymethyl-1,3,4-oxathiazol-2-one

生成物 1

HCID 218503733-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

試薬・触媒・溶媒 1

HCID 8182Dodecane溶媒

反応条件

温度
150 °C

実験手順

4-Methylbenzenesulfonyl cyanide (16.26 g) was added to an emulsion of 5-methoxymethyl-1,3,4-oxathiazol-2-one (6.6 g) in dodecane (60 cm3). The reaction mixture was stirred and heated at 150° C. for 18 hours, then cooled. Water was added and the product extracted into ethyl acetate. The combined organic phases were dried (MgSO4) and ethyl acetate was removed by evaporation under reduced pressure. The residue separated into a brown liquid and a clear dodecane layer which was removed and discarded. Chromatography of the brown liquid on silica gel (Sorbsil C30) using 3:7 ethyl acetate:hexane as eluant give a pale orange oil which solidified on standing (6.94 g). M+ =284; 1H NMR: δ 2.40(3H,s); 3.45(3H,s); 4.7(2H,s); 7.4(2H,d); 8.0(2H,d); (mp 43.4-45-4° C.).

後処理

  1. temperaturecooled
  2. extractionthe product extracted into ethyl acetate
  3. dry with materialThe combined organic phases were dried (MgSO4) and ethyl acetate
  4. customwas removed by evaporation under reduced pressure
  5. customThe residue separated into a brown liquid
  6. customa clear dodecane layer which was removed
  7. customhexane as eluant give a pale orange oil which
  8. custom(mp 43.4-45-4° C.)

出典と根拠

ORDレコード
ord-1870628798e8491aad2820e66a60204b
出典データセット
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05912243

反応ノート

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