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Water → Benzoic acid, 4-(acetylamino)-2-hydroxy-3-(2-propenyl)-, methyl ester

HRID 1084943
ノート
印刷プレビュー

反応式

HRID 1084943 の反応式
C([O:4][C:5]1[CH:14]=[C:13]([NH:15][C:16]([CH3:18])=[O:17])[CH:12]=[CH:11][C:6]=1[C:7]([O:9][CH3:10])=[O:8])C=C.O.CN1C[CH2:24][CH2:23][C:22]1=O>>[OH:4][C:5]1[C:14]([CH2:24][CH:23]=[CH2:22])=[C:13]([NH:15][C:16]([CH3:18])=[O:17])[CH:12]=[CH:11][C:6]=1[C:7]([O:9][CH3:10])=[O:8]
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 962WaterHCID 13387N-methyl-2-pyrrolidone2 回HCID 10586690HCID 10586690、化合物2 回

生成物 1

HCID 10800613Benzoic acid, 4-(acetylamino)-2-hydroxy-3-(2-propenyl)-, methyl ester

実験手順

84 g of methyl 2-allyloxy-4-acetaminobenzoate and 84 g of N-methylpyrrolidone were introduced into a 500 ml round-bottomed flask. The contents were heated quickly to reflux which was then maintained for 30 minutes, and the solution was then cooled slightly and poured into water. Crystallation was immediate. The same operations were repeated with the same quantities of methyl 2-allyloxy-4-acetaminobenzoate and N-methylpyrrolidone and the products from the two trials were combined and cooled, drained, washed with water and dried at 50° C.

後処理

  1. temperatureThe contents were heated quickly
  2. temperatureto reflux which
  3. temperaturewas then maintained for 30 minutes
  4. temperaturethe solution was then cooled slightly
  5. temperaturecooled
  6. washwashed with water
  7. customdried at 50° C.

出典と根拠

ORDレコード
ord-e8b5768364bb496f8a1b6f690452ecad
出典データセット
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05006570

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