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Dimethyl Sulfoxide → 3-Chloro-4-methanesulfonyl-benzaldehyde

HRID 1532274
ノート
印刷プレビュー

反応式

HRID 1532274 の反応式
F[C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[Cl:10].CS(C)=O.[Na+].[CH3:16][S:17]([O-:19])=[O:18]>O>[Cl:10][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:2]=1[S:17]([CH3:16])(=[O:19])=[O:18])[CH:6]=[O:7]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 679Dimethyl SulfoxideHCID 5938663-Chloro-4-fluorobenzaldehydeHCID 2733271Sodium methanesulfinate

生成物 1

HCID 117361153-Chloro-4-methanesulfonyl-benzaldehyde

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
90 °C

実験手順

To a solution containing 1.0 g 4-fluoro-3-chlorobenzaldehyde and 45 ml DMSO, was added 1.93 g methanesulfinic acid sodium salt with stirring at 90° C. The solution was stirred 6 hours at 90° C. and poured into water. Sodiumhydrogencarbonate was added and the product was extracted with ethyl acetate. The extract was evaporated to dryness in vacuo. The residue was triturated with 2-propanol, yield 1.06 g. 1H-NMR (DMSO-d6, 400 MHz): 3.45 (s, 3H, CH3), 8.09-8.27 (m, 3 H, Ar), 10.01 (d, 1 H, CHO).

後処理

  1. stirringThe solution was stirred 6 hours at 90° C.
  2. additionSodiumhydrogencarbonate was added
  3. extractionthe product was extracted with ethyl acetate
  4. customThe extract was evaporated to dryness in vacuo
  5. customThe residue was triturated with 2-propanol, yield 1.06 g

出典と根拠

ORDレコード
ord-83d21be7db304f88a86ee19ac757fb32
出典データセット
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06201027B1

反応ノート

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