2,6-Lutidine → 2,6-Lutidine hydrochloride

HRID 1828766

反応式

HRID 1828766 の反応式
[N:1]1[C:6]([CH3:7])=[CH:5][CH:4]=[CH:3][C:2]=1[CH3:8].C1(S([Cl:23])(=O)=O)C(F)=C(F)C(F)=C(F)C=1F.S(Cl)(Cl)(=O)=O>CC(C)=O.NC1C=CC=CC=1>[ClH:23].[N:1]1[C:6]([CH3:7])=[CH:5][CH:4]=[CH:3][C:2]=1[CH3:8]

参加物

6

反応物 3

HCID 79372,6-LutidineHCID 24648Sulfuryl chlorideHCID 700262,3,4,5,6-Pentafluorobenzenesulfonyl chloride

生成物 1

HCID 5191162,6-Lutidine hydrochloride

試薬・触媒・溶媒 2

HCID 180Acetone溶媒HCID 6115Aniline溶媒2 回

実験手順

Aniline 9.3 (44.6 g, 268 ummol) and 2,6-lutidine (32.8 mL, 282 mmol) were dissolved in 800 mL of acetone (the aniline only partly dissolved). An addition funnel was charged with C6F5SO2Cl (41.8 mL, 282 mmol) and the sulfonyl chloride was added over 15 minutes. During the addition, the starting material dissolved and a new precipitate (2,6-lutidine hydrochloride) formed. After 30 minutes, the 2,6-lutidine hydrochloride was removed by filtration and the filtrate concentrated under reduced pressure. The brown oily solid so produced was triturated with CH2Cl2 and the solid collected. A second batch of product was obtained by repeating the concentration, trituration, and filtration. After drying under high vacuum, 95.5 g (90%) of sulfonamide 9.4 was obtained as a pale yellow solid.

後処理

  1. dissolutiononly partly dissolved)
  2. additionDuring the addition
  3. dissolutionthe starting material dissolved

出典と根拠

ORDレコード
ord-9958b9d1a02643e38c9dc51a0d9d7c95
出典データセット
uspto-grants-2006_06
特許番号
US07060718B2

関連ノート

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