Formic Acid → Benzoic acid, 3-(methylamino)-, methyl ester

HRID 1097054ノート

反応式

HRID 1097054 の反応式
[CH:1](O)=O.C(OC(=O)C)(=O)C.[NH2:11][C:12]1[CH:13]=[C:14]([CH:19]=[CH:20][CH:21]=1)[C:15]([O:17][CH3:18])=[O:16].CSC.B>C1COCC1.CO>[CH3:1][NH:11][C:12]1[CH:13]=[C:14]([CH:19]=[CH:20][CH:21]=1)[C:15]([O:17][CH3:18])=[O:16]

参加物

7

反応物 4

HCID 284Formic AcidHCID 7918Acetic AnhydrideHCID 78274Benzoic acid, 3-amino-, methyl esterHCID 12423031(Dimethyl sulfide)trihydroboron

生成物 1

HCID 10899041Benzoic acid, 3-(methylamino)-, methyl ester

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

A solution of formic acid (106 mL) and acetic anhydride (53.0 mL) was stirred at room temperature for 1 h. Methyl 3-aminobenzoate (8.50 g, 56.2 mmol) was added and the resulting mixture was stirred overnight. The reaction mixture was then concentrated under reduced pressure to give a solid. The solid was dissolved in THF (50.0 mL) and this solution was cooled to 0° C. Borane dimethylsulfide (10.7 mL, 112 mmol) was added slowly and the resulting mixture was stirred at room temperature overnight. The reaction mixture was then cooled to 0° C. and MeOH (10 mL) was added slowly. This mixture was stirred for 3 hours and then concentrated under reduced pressure to give the title compound, which was used without any further purification.

後処理

  1. concentrationThe reaction mixture was then concentrated under reduced pressure
  2. customto give a solid
  3. stirringthe resulting mixture was stirred at room temperature overnight
  4. temperatureThe reaction mixture was then cooled to 0° C.
  5. stirringThis mixture was stirred for 3 hours
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-e3b6c453bc4c4e2a8a2b8134e0794570
出典データセット
uspto-grants-2012_03
特許番号
US08138345B2

反応ノート

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