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Hydrochloric Acid → HCID 21217019、化合物

HRID 704131
ノート
印刷プレビュー

反応式

HRID 704131 の反応式
C([S:4][CH2:5][C:6]1([CH2:14][CH3:15])[CH2:11][O:10]C(C)(C)[O:8][CH2:7]1)(=O)C.Cl>[OH-].[Na+].CO>[OH:8][CH2:7][C:6]([CH2:11][OH:10])([CH2:14][CH3:15])[CH2:5][SH:4]
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 2

HCID 313Hydrochloric AcidHCID 200755985-Acetylthiomethyl-5-ethyl-2,2-dimethyl-1,3-dioxane

生成物 1

HCID 21217019HCID 21217019、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

and (iii) 5-Acetylthiomethyl-5-ethyl-2,2-dimethyl-1,3-dioxane (2.0 g.) was stirred at 20°, in 10% aqueous sodium hydroxide solution (2.0 ml.) in methanol (20 ml.), for 24 hours under nitrogen. The mixture was neutralized with concentrated hydrochloric acid (0.5 ml.). Dowex 50×8-200 ion exchange resin (H+ form) (1.0 g.) was added and the mixture was refluxed with stirring, under nitrogen, for 4 hours. The mixture was filtered and the filtrate was evaporated in vacuo. Toluene was added to the residue and the mixture was evaporated in vacuo. 2,2-Di-(hydroxymethyl)-butanethiol was obtained as a colourless oil and was used without further purification (1.0 g.)

後処理

  1. additionDowex 50×8-200 ion exchange resin (H+ form) (1.0 g.) was added
  2. temperaturethe mixture was refluxed
  3. filtrationThe mixture was filtered
  4. customthe filtrate was evaporated in vacuo
  5. additionToluene was added to the residue
  6. customthe mixture was evaporated in vacuo

出典と根拠

ORDレコード
ord-b9bcf293efee4f6092d44c5086b50fe0
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04985582

反応ノート

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