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Hydrochloric Acid → 3-methyl-N-(2-methylphenoxyacetyl)anthranilic acid

HRID 1587421
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반응식

HRID 1587421 반응식
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:4]([C:5]([OH:7])=[O:6])[C:3]=1[NH2:11].[CH3:12][C:13]1[CH:23]=[CH:22][CH:21]=[CH:20][C:14]=1[O:15][CH2:16][C:17](Cl)=[O:18].Cl>[OH-].[Na+]>[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:4]([C:5]([OH:7])=[O:6])[C:3]=1[NH:11][C:17](=[O:18])[CH2:16][O:15][C:14]1[CH:20]=[CH:21][CH:22]=[CH:23][C:13]=1[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 781012-Amino-3-methylbenzoic acidHCID 12353488(2-Methylphenoxy)acetyl chloride

생성물 1

HCID 197577613-methyl-N-(2-methylphenoxyacetyl)anthranilic acid수율 94.7%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

3-Methylanthranilic acid 1.0 g (6 mmol) was dissolved in 10% aqueous sodium hydroxide solution 27 ml and to this soulution, 2-methylphenoxyacetyl chloride 1.3 g (7.3 mmol) was added dropwise at 0° C. The resulting solution was stirred at room temperature for 5 minutes and acidified with 10% hydrochloric acid solution. Deposited crystals were collected by filtration, washed with hot water and recrystallized from ethanol to obtain 3-methyl-N-(2-methylphenoxyacetyl)anthranilic acid (melting point: 133° to 136° C.) 1.7 g (yield: 83%).

후처리

  1. additionwas added dropwise at 0° C
  2. filtrationDeposited crystals were collected by filtration
  3. washwashed with hot water
  4. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-983cc726145b4ca9a6c36fb503f52212
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05217961

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