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Potassium → diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)propylphosphonate

HRID 1706180
ノート
印刷プレビュー

反応式

HRID 1706180 の反応式
Cl[CH2:2][CH2:3][CH2:4][P:5](=[O:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8].[K].[CH2:14]([O:16][C:17]([O:19][NH:20][C:21](=[O:25])[O:22][CH2:23][CH3:24])=[O:18])[CH3:15]>CN(C)C=O>[CH2:23]([O:22][C:21]([N:20]([CH2:2][CH2:3][CH2:4][P:5](=[O:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8])[O:19][C:17]([O:16][CH2:14][CH3:15])=[O:18])=[O:25])[CH3:24]
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 5462222PotassiumHCID 11446651Ethyl EthoxycarbonyloxycarbamateHCID 133232971-Chloro-3-diethoxyphosphoryl-propane

生成物 1

HCID 20337213diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)propylphosphonate収率 90.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of diethyl 3-chloropropylphosphonate (430.6 g) in dry N,N-dimethylformamide (2.25 l) was added potassium salt of ethyl N-ethoxycarbonyloxycarbamate (429.2 g). This mixture was stirred at 64°-66° C. for three hours. After the resulting potassium chloride was removed by filtration, the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (2.0 l) and washed with water (4.0 l). The aqueous layer was extracted twice with ethyl acetate (1.2 and 0.8 l). The combined ethyl acetate layer was washed with saturated aqueous sodium chloride solution (1.5 l), dried over magnesium sulfate and concentrated under reduced pressure to give oily diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)-propylphosphonate (643.7 g).

後処理

  1. customAfter the resulting potassium chloride was removed by filtration
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. dissolutionThe residue was dissolved in ethyl acetate (2.0 l)
  4. washwashed with water (4.0 l)
  5. extractionThe aqueous layer was extracted twice with ethyl acetate (1.2 and 0.8 l)
  6. washThe combined ethyl acetate layer was washed with saturated aqueous sodium chloride solution (1.5 l)
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-3c9035176e104eee9d3c7f23936fa107
出典データセット
uspto-grants-1980_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04206156

反応ノート

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