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

HRID 323783

反応式

HRID 323783 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 mmol) 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-e685f8520597489c906543d6701410b5
出典データセット
uspto-grants-2001_04
特許番号
US06214880B1

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