Tetrabutylammonium Fluoride → 2-Chloro-5-ethynylpyridine

HRID 1350640ノート

反応式

HRID 1350640 の反応式
CCCC[N+](CCCC)(CCCC)CCCC.[F-].[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]#[C:27][Si](C)(C)C)=[CH:22][N:21]=1>C1COCC1>[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]#[CH:27])=[CH:22][N:21]=1

参加物

4

反応物 2

HCID 2724141Tetrabutylammonium FluorideHCID 106322252-Chloro-5-trimethylsilanylethynyl-pyridine

生成物 1

HCID 106542812-Chloro-5-ethynylpyridine収率 73.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A 1 M solution of TBAF in THF (12 mL) was added to 500 mg (2.38 mmol) of 2-chloro-5-trimethylsilanylethynyl-pyridine and the black solution was stirred overnight. The mixture was concentrated, the resulting residue was stirred in 50 mL of Et2O for 1 h, and the liquid was decanted from the solids. This washing procedure was repeated twice, and the combined washes were concentrated and chromatographed to provide 240 mg of 2-chloro-5-ethynylpyridine as a colorless solid.

後処理

  1. concentrationThe mixture was concentrated
  2. stirringthe resulting residue was stirred in 50 mL of Et2O for 1 h
  3. customthe liquid was decanted from the solids
  4. concentrationthe combined washes were concentrated
  5. customchromatographed

出典と根拠

ORDレコード
ord-7c23a5adb5da4f83975cf76acaeb44d1
出典データセット
uspto-grants-2007_05
特許番号
US07214802B2

反応ノート

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