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Hydrochloric Acid → 3-amino-4-(methylcarbamoyl)benzoic Acid

HRID 1451115
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HRID 1451115 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[C:12]([NH:14][CH3:15])=[O:13])[C:5]([O:7]C)=[O:6].[OH-].[Na+].Cl>C(O)(=O)C>[NH2:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[C:12]([NH:14][CH3:15])=[O:13])[C:5]([OH:7])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 10798400Methyl 3-amino-4-(methylcarbamoyl)benzoate

생성물 1

HCID 104201413-amino-4-(methylcarbamoyl)benzoic Acid수율 69%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of methyl 3-amino-4-(methylamino)carbonylbenzoate (0.624 g, 0.003 mol) and 1N sodium hydroxide (4.5 mol, 0.0045 mol) was stirred at room temperature for 4 h. The mixture was neutralized with concentrated hydrochloric acid and then acetic acid was added to bring the pH close to 3. The precipitate obtained was collected by filtration, washed with water, and dried under vacuum over acetone for 24 h to give 0.4 g (69%) of 3-amino-4-(methylamino)carbonylbenzoic acid as a pale yellow powder, mp 215°-217° C.

후처리

  1. customclose to 3
  2. customThe precipitate obtained
  3. filtrationwas collected by filtration
  4. washwashed with water
  5. dry with materialdried under vacuum over acetone for 24 h

출처 및 근거

ORD 기록
ord-2c6a40e6e46944d48ca1a4586a668851
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05602277

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