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Methyl 2-benzamido-2-(4-methoxycarbonyl-3-methoxy-6-methylphenyl)acetate → 4-(amino-carboxy-methyl)-2-hydroxy-5-methyl-benzoic Acid

HRID 343953
ノート
印刷プレビュー

反応式

HRID 343953 の反応式
C([NH:9][CH:10]([C:15]1[C:20]([CH3:21])=[CH:19][C:18]([C:22]([O:24]C)=[O:23])=[C:17]([O:26]C)[CH:16]=1)[C:11]([O:13]C)=[O:12])(=O)C1C=CC=CC=1>Cl>[C:22]([C:18]1[CH:19]=[C:20]([CH3:21])[C:15]([CH:10]([C:11]([OH:13])=[O:12])[NH2:9])=[CH:16][C:17]=1[OH:26])([OH:24])=[O:23]
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 54245466Methyl 2-benzamido-2-(4-methoxycarbonyl-3-methoxy-6-methylphenyl)acetate

生成物 1

HCID 100365994-(amino-carboxy-methyl)-2-hydroxy-5-methyl-benzoic Acid

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

A stirred suspension of methyl 2-benzamido-2-(4-methoxycarbonyl-3-methoxy-6-methylphenyl)acetate (120 mg, 0.32 mmol) in aqueous hydrochloric acid (5M, 3 ml) was heated to 110° C. for 7 days in a PTFE lined stainless steel sealed reaction vessel. The contents were periodically cooled, evaporated and topped up with an equivalent amount of fresh aqueous hydrochloric acid. The contents were cooled and chromatographed on ion exchange resin following the procedure described in Example 1 (iii) to give the title compound as an off-white solid, m.p. >250° C.

後処理

  1. customsealed
  2. customreaction vessel
  3. temperatureThe contents were periodically cooled
  4. customevaporated
  5. temperatureThe contents were cooled
  6. customchromatographed on ion exchange resin

出典と根拠

ORDレコード
ord-32942008bd02400897c07b71e116579d
出典データセット
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05863947

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート