Butanal → 2-Ethyl-4-methyl-1,3-oxathiane

HRID 1907130

反応式

HRID 1907130 の反応式
[SH:1][CH:2]([CH3:6])[CH2:3][CH2:4][OH:5].[CH3:7][C:8]1C=CC(S(O)(=O)=O)=C[CH:13]=1.C(=O)CCC>C(Cl)Cl>[CH2:8]([CH:13]1[S:1][CH:2]([CH3:6])[CH2:3][CH2:4][O:5]1)[CH3:7]

参加物

5

実験手順

A solution of 3-mercapto-1-butanol (106 g, 1 mol, synthesized as above) and PTSA (paratoluenesulfonic acid monohydrate, 38 g, 0.2 mol, commercially available from Sigma-Aldrich, Inc.) in 400 mL of CH2Cl2 (dichloromethane) were cooled with an ice bath. Butyraldehyde (106 mL, 1.2 mol, commercially available from Sigma-Aldrich, Inc.) was added drop wise to the solution, and the reaction mixture was stirred with cooling for half an hour and at room temperature for another 1 hour. The reaction mixture was washed twice with saturated sodium bicarbonate solution and once with brine. The organic phase was then dried with anhydrous magnesium sulfate. The solvent was removed with a rotary evaporator and the crude product was distilled under vacuum to provide 2-ethyl-4-methyl-1,3-oxathiane (98 g), which had a boiling point of 80° C. at a pressure of 10.4 mmHg.

後処理

  1. addition) was added drop wise to the solution
  2. washThe reaction mixture was washed twice with saturated sodium bicarbonate solution and once with brine
  3. dry with materialThe organic phase was then dried with anhydrous magnesium sulfate
  4. customThe solvent was removed with a rotary evaporator
  5. distillationthe crude product was distilled under vacuum

出典と根拠

ORDレコード
ord-511aac09fa314a5f967c78ef6433e16c
出典データセット
uspto-grants-2013_12
特許番号
US08598110B2

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