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Triacetoxyperiodinane → HCID 59540695、化合物

HRID 1677409
ノート
印刷プレビュー

反応式

HRID 1677409 の反応式
[F:1][C:2]([F:12])([F:11])[C:3]([CH3:10])([C:6]([F:9])([F:8])[F:7])[CH2:4][OH:5].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>>[F:1][C:2]([F:11])([F:12])[C:3]([CH3:10])([C:6]([F:7])([F:9])[F:8])[CH:4]=[O:5]
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

3

反応物 2

HCID 159087TriacetoxyperiodinaneHCID 27361853,3,3-Trifluoro-2-methyl-2-(trifluoromethyl)propan-1-ol

生成物 1

HCID 59540695HCID 59540695、化合物

反応条件

温度
100 °C

実験手順

3,3,3-Trifluoro-2-methyl-2-trifluoromethyl-propan-1-ol, 1 gm, 5.1 mM, and Dess-Martin Periodinane, 4.3 gm, 10.2 mM, 2 eq. was added to ten ml of 1,1,1,3 tetrachloroethane and the mixture stirred for several hours. A short path distillation head was added and the receiver flask was cooled in dry ice-acetone bath. The mixture was heated to 100° C. and the pressure lowered to 180 Ton. The desired product 3,3,3-Trifluoro-2-methyl-2-trifluoromethyl-propionaldehyde condensed in the receiver flask and was used without further purification in the above reaction.

後処理

  1. distillationA short path distillation head
  2. additionwas added
  3. temperaturethe receiver flask was cooled in dry ice-acetone bath
  4. customThe desired product 3,3,3-Trifluoro-2-methyl-2-trifluoromethyl-propionaldehyde condensed in the receiver flask
  5. customwas used without further purification in the above reaction

出典と根拠

ORDレコード
ord-e704309765e7428b8be03d1f1c6a7df3
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08008298B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート