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

HRID 1632240
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반응식

HRID 1632240 반응식
[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]
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 12958Dimethyl methylphosphonateHCID 178418339Butyllithium

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-e146ff3869ee4237a5e25089f99bfffe
출처 데이터셋
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04474802

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