Ammonia → 3-Methoxymethoxy-2,2-dimethylpropionic acid methoxymethyl ester

HRID 2089622ノート

反応式

HRID 2089622 の反応式
[OH:1][CH2:2][C:3]([CH3:8])([CH3:7])[C:4]([OH:6])=[O:5].[CH3:9][O:10][CH2:11]Cl.C(N(CC)C(C)C)(C)C.N.Cl.[CH2:24]([O:26][CH2:27]C)C>ClCCl>[CH3:9][O:10][CH2:11][O:5][C:4](=[O:6])[C:3]([CH3:8])([CH3:7])[CH2:2][O:1][CH2:24][O:26][CH3:27]

参加物

8

実験手順

To a mixture of 3-hydroxy-2,2-dimethylpropionic acid [CAS No. 4835-90-9] (10 g) and dichloromethane (350 mL), at 0° C., chloromethyl methyl ether (16.1 mL) dissolved in dichloromethane (30 mL) and N,N-diisopropylethylamine (44.2 mL) were sequentially added. After stirring the mixture overnight at room temperature, aqueous ammonia (50 mL) was added thereto. To the mixture, 2 N hydrochloric acid (500 mL) and diethyl ether (800 mL) were added, and the resulting mixture was shaken, followed by collection of the organic layer. The organic layer was sequentially washed with saturated aqueous sodium hydrogen carbonate solution (300 mL) and saturated aqueous sodium chloride solution (300 mL), and dried over anhydrous magnesium sulfate. The resulting mixture was filtered and the obtained filtrate was concentrated under reduced pressure to obtain the captioned compound (16.5 g).

後処理

  1. stirringthe resulting mixture was shaken
  2. customfollowed by collection of the organic layer
  3. washThe organic layer was sequentially washed with saturated aqueous sodium hydrogen carbonate solution (300 mL) and saturated aqueous sodium chloride solution (300 mL)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationThe resulting mixture was filtered
  6. concentrationthe obtained filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-605a99eafd66449c83cf22766bf4b26d
出典データセット
uspto-grants-2013_05
特許番号
US08436009B2

反応ノート

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