Sodium hydride → 2-(3,4-Dihydro-2H-4-chromenylidene)acetonitrile

HRID 428173

反応式

HRID 428173 の反応式
[C:1]([CH2:3]P(=O)(OCC)OCC)#[N:2].[H-].[Na+].[O:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:17](=O)[CH2:16][CH2:15]1>O1CCCC1>[O:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:17](=[CH:3][C:1]#[N:2])[CH2:16][CH2:15]1

参加物

5

反応物 3

HCID 24758Sodium hydrideHCID 68110ChromanoneHCID 75676Diethyl (cyanomethyl)phosphonate

生成物 1

HCID 569848342-(3,4-Dihydro-2H-4-chromenylidene)acetonitrile

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

Diethyl cyanomethylphosphonate (1.15 eq.) is slowly added to a suspension of sodium hydride (1.15 eq.) in anhydrous tetrahydrofuran at 0° C. The reaction medium is stirred for 10 minutes at 0° C. and then cooled to −78° C. 4-Chromanone dissolved in tetrahydrofuran is added. The temperature is then returned slowly to 20-25° C. over 2 hours 30. After removal of the solvent, the compounds are extracted with ethyl acetate. The organic phase is washed with a large amount of a saturated solution of sodium chloride, concentrated and purified (Z/E mixture) on a silica column (AcOEt/PE 3/7).

後処理

  1. temperaturecooled to −78° C
  2. additionis added
  3. waitThe temperature is then returned slowly to 20-25° C. over 2 hours
  4. customAfter removal of the solvent
  5. extractionthe compounds are extracted with ethyl acetate
  6. washThe organic phase is washed with a large amount of a saturated solution of sodium chloride
  7. concentrationconcentrated
  8. custompurified (Z/E mixture) on a silica column (AcOEt/PE 3/7)

出典と根拠

ORDレコード
ord-a8d847581f8746b59b832d47f4769ed2
出典データセット
uspto-grants-2001_11
特許番号
US06313160B1

関連ノート

読み込み中…