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Diethyl Ether → Dimethyl (2-oxohept-5-yn-1-yl)phosphonate

HRID 1632240
ノート
印刷プレビュー

反応式

HRID 1632240 の反応式
[CH3:1][P:2]([O:6][CH3:7])(=[O:5])[O:3][CH3:4].[CH2:8]([Li])[CH2:9][CH2:10][CH3:11].CC[O:15][CH2:16][CH3:17]>O1CCCC1>[O:15]=[C:16]([CH2:17][CH2:8][C:9]#[C:10][CH3:11])[CH2:1][P:2]([O:6][CH3:7])(=[O:5])[O:3][CH3:4]
参加物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 3283Diethyl EtherHCID 12958Dimethyl methylphosphonateHCID 178418339Butyllithium

生成物 1

HCID 13269871Dimethyl (2-oxohept-5-yn-1-yl)phosphonate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of 3.2 g of dimethyl methanephosphonate in 52 ml of tetrahydrofuran was added at -78° C. 155 ml of n-butyl lithium (1.59N) and the mixture was stirred for 25 mins at -78° C. To the mixture was added at -78° C. a solution of 1.6 g of the above-mentioned ester in 3.2 ml of tetrahydrofuran. The mixture was stirred for 15 mins and for one hour at room temperature. After addition of 100 ml of ether to the reaction mixture, the mixture was washed with 30 ml of aqueous saturated solution of oxalic acid, 50 ml of water and 40 ml of aqueous saturated solution of sodium chloride. The washed mixture was dried and concentrated to give an oily material. The oily material was distilled under reduced pressure to yield 2.2 g of dimethyl 2-oxo-hept-5-yne-phosphonate (143° to 146° C./0.7 mmHg).

後処理

  1. washthe mixture was washed with 30 ml of aqueous saturated solution of oxalic acid, 50 ml of water and 40 ml of aqueous saturated solution of sodium chloride
  2. customThe washed mixture was dried
  3. concentrationconcentrated
  4. customto give an oily material
  5. distillationThe oily material was distilled under reduced pressure

出典と根拠

ORDレコード
ord-e146ff3869ee4237a5e25089f99bfffe
出典データセット
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04474802

反応ノート

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