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Ethyl 3-amino-2-methylpropyl(diethoxymethyl)phosphinate → 3-Amino-2-methylpropylphosphonous acid monohydrate

HRID 622874
ノート
印刷プレビュー

反応式

HRID 622874 の反応式
[NH2:1][CH2:2][CH:3]([CH3:17])[CH2:4][P:5](C(OCC)OCC)(=[O:9])[O:6]CC>Cl>[OH2:6].[NH2:1][CH2:2][CH:3]([CH3:17])[CH2:4][P:5]([OH:9])[OH:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 14362817Ethyl 3-amino-2-methylpropyl(diethoxymethyl)phosphinate

生成物 1

HCID 867414053-Amino-2-methylpropylphosphonous acid monohydrate

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

A solution of 6.0 g of ethyl 3-amino-2-methylpropyl(diethoxymethyl)phosphinate in 30 ml of 36% aqueous hydrochloric acid is heated to reflux for a period of 7 hours. The reaction mixture is then allowed to cool to room temperature, concentrated under reduced pressure and co-evaporated twice with 10 ml water under reduced pressure and co-evaporated twice with 10 ml of water under reduced pressure. The crude product is dissolved in 50 ml of dry ethanol and 5 ml of propylene oxide is added dropwise. The precipitated solid is collected by filtration and dried to give 3-amino-2-methylpropylphosphonous acid monohydrate, m.p. 96°-100° C., 31P=+25.8 ppm (D2O).

後処理

  1. temperatureto reflux for a period of 7 hours
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe crude product is dissolved in 50 ml of dry ethanol
  4. addition5 ml of propylene oxide is added dropwise
  5. filtrationThe precipitated solid is collected by filtration
  6. customdried

出典と根拠

ORDレコード
ord-568ded0d150d452da6c7c01ba637ea25
出典データセット
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04772738

反応ノート

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