ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Iodoethylene → 1,1,1-Trifluoro-2-(2-mercapto-1,3-thiazol-5-yl)but-3-en-2-ol

HRID 2116663
ノート
印刷プレビュー

反応式

HRID 2116663 の反応式
[CH:1](I)=[CH2:2].C([Li])(C)(C)C.[F:9][C:10]([F:20])([F:19])[C:11]([C:13]1[S:17][C:16]([SH:18])=[N:15][CH:14]=1)=[O:12]>CCOCC>[F:20][C:10]([F:9])([F:19])[C:11]([C:13]1[S:17][C:16]([SH:18])=[N:15][CH:14]=1)([OH:12])[CH:1]=[CH2:2]
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 68976IodoethyleneHCID 178418306HCID 178418306、化合物HCID 178519847HCID 178519847、化合物

生成物 1

HCID 1784588031,1,1-Trifluoro-2-(2-mercapto-1,3-thiazol-5-yl)but-3-en-2-ol

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
-78 °C

実験手順

To a solution of vinyl iodide (1.88 g, 12.2 mmol) in Et2O at −78° C. was added t-butyl lithium (14.3 ml, 1.7 M/pentane, 24.3 mmol). The mixture was stirred at −78° C. for 1 h and warmed up to −30° C. for 5 min. The mixture was cooled back to −78° C. and 2,2,2-trifluoro-1-(2-mercapto-1,3-thiazol-5-yl)ethanone (1.18 g, 5.53 mmol) in Et2O was added. The reaction mixture stirred 30 min at −78° C., brought to 0° C. and partitioned between aqueous NH4Cl and EtOAc. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine and dried over anhydrous Na2SO4. The solvent was evaporated and the residue chromatographed on silica gel (toluene/acetone; 90:10) to give the title compound.

後処理

  1. temperaturewarmed up to −30° C. for 5 min
  2. temperatureThe mixture was cooled back to −78° C.
  3. stirringThe reaction mixture stirred 30 min at −78° C.
  4. custombrought to 0° C.
  5. custompartitioned between aqueous NH4Cl and EtOAc
  6. customThe layers were separated
  7. extractionthe aqueous phase was extracted with EtOAc
  8. washThe combined organic layers were washed with brine
  9. dry with materialdried over anhydrous Na2SO4
  10. customThe solvent was evaporated
  11. customthe residue chromatographed on silica gel (toluene/acetone; 90:10)

出典と根拠

ORDレコード
ord-6688bbe9cb174e38b23a8b7707a6b987
出典データセット
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07439260B2

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