Hydrochloric Acid → HCID 53869197、化合物

HRID 488110

反応式

HRID 488110 の反応式
[C:1]1([CH2:7][NH:8][C:9](=[O:11])[CH3:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([N-][CH:16]([CH3:18])[CH3:17])(C)C.[Li+].[C:20]([CH2:22][C@@H:23]([OH:30])[CH2:24][C:25](OCC)=[O:26])#[N:21].Cl.O1CCC[CH2:33]1>O1CCCC1.CCCCCCC>[C:20]([CH2:22][C@@H:23]([OH:30])[CH2:24][C:25](=[O:26])[CH2:10][C:9]([N:8]([C:16]([CH3:17])([CH3:18])[CH3:33])[CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:11])#[N:21]

参加物

7

実験手順

To a stirred -10° C. solution of N-1,1-dimethyl-ethyl, N-phenylmethylacetamide (prepared from N-1,1-dimethylethyl, N-phenylmethyl amine, and acetyl chloride by refluxing for 2 hours in toluene) (102.5 g, 0.5 mol) in tetrahydrofuran (0.5 L) is slowly added a solution of lithium diisopropylamide in tetrahydrofuran-heptane (0.25 L of 2M) while maintaining the temperature between -40° C. to -50° C., and the mixture is stirred at -20° C. to -30° C. for 30 minutes. (R)-4-cyano-3-hydroxybutyric acid, ethyl ester (Brower, supra) (20 g, 0.125 mol) as a solution in 200 mL or tetrahydrofuran is then added to the previous mixture. The reaction mixture is stirred for 30 minutes at -25° C. to -20° C., and transferred to a 2.2N aqueous hydrochloric acid solution (0.5 L). The aqueous layer is extracted with 300 mL of ethyl acetate, the aqueous layer is separated and reextracted with 100 mL of ethyl acetate, the extracts are combined and concentrated in vacuo to afford crude (R)-6-cyano-N-(1,1-dimethylethyl)-5-hydroxy-3-oxo-N-(phenylmethyl)hexanamide as an oil.

後処理

  1. temperaturewhile maintaining the temperature between -40° C. to -50° C.
  2. stirringThe reaction mixture is stirred for 30 minutes at -25° C. to -20° C.
  3. extractionThe aqueous layer is extracted with 300 mL of ethyl acetate
  4. customthe aqueous layer is separated
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ab378d00d9d4494796b6c0db5e6972e8
出典データセット
uspto-grants-1994_03
特許番号
US05298627

関連ノート

読み込み中…