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Carbon Dioxide → 1-Methyl-1-oxo-1lambda5-phosphinane-4-carboxylic acid

HRID 1863890
ノート
印刷プレビュー

反応式

HRID 1863890 の反応式
[CH3:1][P:2]1(=[O:14])[CH2:7][CH2:6][C:5](C(O)=O)([C:8]([OH:10])=[O:9])[CH2:4][CH2:3]1.C(=O)=O>O>[CH3:1][P:2]1(=[O:14])[CH2:7][CH2:6][CH:5]([C:8]([OH:10])=[O:9])[CH2:4][CH2:3]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 280Carbon DioxideHCID 579732941-Methyl-1-oxo-1lambda5-phosphinane-4,4-dicarboxylic acid

生成物 1

HCID 579733021-Methyl-1-oxo-1lambda5-phosphinane-4-carboxylic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
215 °C

実験手順

To a 50 mL microwave pressure flask equipped with a stir-bar was added 1-methyl-1-oxo-1λ5-phosphinane-4,4-dicarboxylic acid (0.25 g, 5.7 mmol) and water (20 mL) to give a suspension. The flask was sealed and heated to 215° C. over 60 seconds, at which point a pressure spike was observed. The flask was allowed to cool to room temperature then vented to release pressure from dissolved CO2. The resulting clear and colorless solution was concentrated by lyophilization to provide 1-methyl-1-oxo-1λ5-phosphinane-4-carboxylic acid in quantitative yield as a mixture of cis/trans isomers (˜2:1; identity of the favored isomer not determined). 1H NMR (400 MHz, D2O) δ ppm 2.6-2.4 (m, 1H), 2.2-1.6 (m, 8H), 1.48 (d, J=12.9 Hz, minor isomer, 1H), 1.44 (d, J=13.7 Hz, major isomer, 2H); ESMS m/z: found, 177 (M+1)+, 353 (2M+1)+.

後処理

  1. customTo a 50 mL microwave pressure flask equipped with a stir-bar
  2. customto give a suspension
  3. customThe flask was sealed
  4. temperatureto cool to room temperature
  5. concentrationThe resulting clear and colorless solution was concentrated by lyophilization

出典と根拠

ORDレコード
ord-ba9586c191e84311abb32419dadfb91e
出典データセット
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07625880B2

反応ノート

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