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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Chloroacetic Acid → 2-(Chloromethyl)-1-methylbenzimidazole

HRID 253473
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인쇄 미리보기

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HRID 253473 반응식
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[NH2:9].[Cl:10][CH2:11][C:12](O)=O>Cl.O.C(=O)(O)[O-].[Na+]>[Cl:10][CH2:11][C:12]1[N:2]([CH3:1])[C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 300Chloroacetic AcidHCID 78498N-Methyl-o-phenylenediamine

생성물 1

HCID 2480442-(Chloromethyl)-1-methylbenzimidazole수율 87.8%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 962Water용매HCID 516892Sodium Bicarbonate용매

반응 조건

온도
55 °C

실험 절차

N-methyl-phenylenediamine (1 g, 8.2 mmol) and chloroacetic acid (0.9 g, 9.4 mol) were dissolved in 5 N aqueous hydrochloric acid (10 mL) and stirred at 55° C. overnight. The reaction mixture was then diluted with water and basified with solid sodium bicarbonate to give a precipitate which was filtered, washed with water and dried to provide the desired compound (1.3 g, 87%).

후처리

  1. customto give a precipitate which
  2. filtrationwas filtered
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-ba330bcfa33e419daff6496203bb19c7
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07872018B2

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