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Triethylamine → 919482-29-4

HRID 1594159
ノート
印刷プレビュー

反応式

HRID 1594159 の反応式
[CH3:1][C:2]1([CH3:8])[O:6][CH2:5][CH:4]([OH:7])[O:3]1.[CH2:9](N(CC)CC)C.[CH3:16][S:17](Cl)(=[O:19])=[O:18].[Cl-].[NH4+]>O1CCCC1>[CH3:16][S:17]([O:7][CH:4]1[CH2:5][O:6][C:2]([CH3:8])([CH3:1])[O:3][CH2:9]1)(=[O:19])=[O:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 25517Ammonium ChlorideHCID 31297Methanesulfonyl chlorideHCID 155822192,2-Dimethyl-1,3-dioxolan-4-ol

生成物 1

HCID 44189836919482-29-4

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A 2,2-dimethyl-1,3-dioxolan-5-ol (743 mg) solution in tetrahydrofuran (10 mL) was cooled to 0° C. in nitrogen atmosphere. To the reaction mixture, triethylamine (1.87 mL) and methanesulfonyl chloride (520 μL) were successively added at 0° C., followed by 30 minutes' stirring. After addition of saturated aqueous ammonium chloride solution, the reaction mixture was extracted with ethyl acetate. The extract washed with saturated brine, dried over anhydrous magnesium sulfate and the solvent was removed by distillation to provide 837 mg of crude title compound as a colorless solid.

後処理

  1. extractionthe reaction mixture was extracted with ethyl acetate
  2. washThe extract washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was removed by distillation

出典と根拠

ORDレコード
ord-5994f08bc24b4279a61f0e779823fb82
出典データセット
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07300947B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート