反応式
CS(OC(CCCCCCCC)C)(=O)=O.IC1C=C(I)C=C(I)C=1O.C(=O)([O-])[O-].[K+].[K+].[I:32][C:33]1[CH:54]=[C:53]([I:55])[CH:52]=[C:51]([I:56])[C:34]=1[O:35][CH:36]([CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45]CCCCC)[CH3:37]>CN(C=O)C>[I:32][C:33]1[CH:54]=[C:53]([I:55])[CH:52]=[C:51]([I:56])[C:34]=1[O:35][CH:36]([CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45])[CH3:37]参加物
6
実験手順
The 2-methanesulfonyloxydecane (14.8 g, 62.6 mmol), 2,4,6-triiodophenol (29.7 g) 62.9 mmol) and potassium carbonate (8.7 g, 63.0 mmol) were reacted in DMF (210 ml) as per 2-(2,4,6-triiodophenoxy)-pentadecane except at an oil bath temperature of 72° C. for 88 hrs. The reaction was processed as for 2-(2,4,6-triiodophenoxy)-pentadecane to provide a light brown residue. Flash column chromatography (silica, hexanes) provided 2-(2,4,6-triiodophenoxy)-decane (29.1 g, 75.9%) as a white solid.
後処理
- customto provide a light brown residue
出典と根拠
- ORDレコード
- ord-1388a0bb205b46dea30b1e71d3f714ba
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05620677
関連ノート
読み込み中…