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Hydrochloric Acid → HCID 69331765、化合物

HRID 1765986
ノート
印刷プレビュー

反応式

HRID 1765986 の反応式
C([NH:4][C@@H:5]([C:16]([OH:18])=[O:17])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([CH3:13])=[C:9]([O:14][CH3:15])[CH:8]=1)(=O)C.C1(C)C=CC=CC=1.[ClH:26]>>[ClH:26].[CH3:15][O:14][C:9]1[CH:8]=[C:7]([CH:12]=[CH:11][C:10]=1[CH3:13])[CH2:6][C@H:5]([C:16]([OH:18])=[O:17])[NH2:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 313Hydrochloric AcidHCID 1140TolueneHCID 54030461HCID 54030461、化合物

生成物 1

HCID 69331765HCID 69331765、化合物

実験手順

A mixture of N-acetyl-3-methoxy-4-methyl-D-phenylalanine (2.55 g) in a mixture of 6N hydrochloric acid (25.5 ml) with toluene (18 ml) was stirred under reflux for 4 hours. After cooling to room temperature, the aqueous layer was separated and the organic layer was washed twice with water (10 ml). The aqueous layer and the washings were combined and the solvent was evaporated under reduced pressure. The produced crystals were collected by filtration and washed with ice-water to give 3-methoxy-4-methyl-D-phenylalanine hydrochloride (1.35 g) in the form of colorless crystals. The solvent was evaporated from the filtrate under reduced pressure to give crude 3-methoxy-4-methyl-D-phenylalanine hydrochloride (0.6 g).

後処理

  • temperatureunder reflux for 4 hours
  • customthe aqueous layer was separated
  • washthe organic layer was washed twice with water (10 ml)
  • customthe solvent was evaporated under reduced pressure
  • filtrationThe produced crystals were collected by filtration
  • washwashed with ice-water
  • 出典と根拠

    ORDレコード
    ord-0a834d6d19f44ad59a49cf9c800f5927
    出典データセット
    uspto-grants-2007_06
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07229992B2

    反応ノート

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