Diethyl Ether → HCID 178461648、化合物

HRID 249066ノート

反応式

HRID 249066 の反応式
[CH3:1][N:2]([C@@H:4]([C-:6]1[CH:10]=[CH:9][CH:8]=[CH:7]1)[CH3:5])[CH3:3].[CH-:11]1[CH:15]=[CH:14][CH:13]=[CH:12]1.[Fe+2:16].C[I:18].C(OCC)C>CC(C)=O>[I-:18].[CH3:1][N+:2]([C@@H:4]([C-:6]1[CH:10]=[CH:9][CH:8]=[CH:7]1)[CH3:5])([CH3:11])[CH3:3].[CH-:11]1[CH:15]=[CH:14][CH:13]=[CH:12]1.[Fe+2:16]

参加物

5

反応物 3

HCID 3283Diethyl EtherHCID 6328Methyl iodideHCID 15823231cyclopenta-1,3-diene;(1R)-1-cyclopenta-2,4-dien-1-yl-N,N-dimethylethanamine;iron(2+)

生成物 1

HCID 178461648HCID 178461648、化合物収率 200%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

20.0 g (77.8 mmol) of (R)-N,N-dimethyl-1-ferrocenylethylamine was added under argon atmosphere to a glass vessel (atmospheric pressure use only) with an agitator and dissolved in acetone 37 ml. After cooling with ice water, methyl iodide 21 ml (337 mmol) was added to the vessel and reacted for 15 minutes under cooling with ice water. After reaction, ethylether 160 ml was added to the vessel and crystals were deposited. The crystals were collected by filtration to obtain (R)-N,N,N-trimethyl-1-ferrocenylethylammonium iodide 31.0 g (77.8 mmol) (yield: 100%).

後処理

  1. additionwas added to the vessel
  2. customreacted for 15 minutes
  3. additionwas added to the vessel and crystals
  4. filtrationThe crystals were collected by filtration

出典と根拠

ORDレコード
ord-b2cc510d4d24421a975271eb5f6dc29b
出典データセット
uspto-grants-1993_05
特許番号
US05212311

反応ノート

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