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O-Phenylenediamine → 2-Mesitylbenzimidazole

HRID 630555
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인쇄 미리보기

반응식

HRID 630555 반응식
[C:1]1([NH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH2:7].[CH3:9][C:10]1[CH:18]=[C:17]([CH3:19])[CH:16]=[C:15]([CH3:20])[C:11]=1[C:12](O)=O>O>[C:10]1([CH3:9])[CH:18]=[C:17]([CH3:19])[CH:16]=[C:15]([CH3:20])[C:11]=1[C:12]1[NH:7][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[N:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7243O-PhenylenediamineHCID 101942,4,6-Trimethylbenzoic acid

생성물 1

HCID 227347972-Mesitylbenzimidazole

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
150 °C

실험 절차

2-Mesitylbenzimidazole was synthesized by dissolving 1.5 g 1,2-phenylene diamine (14 mmol) in 40 g of PPA at 120° C. To this solution, 2.1 g of 2,4,6-trimethylbenzoic acid (13 mmol) was added and the temperature was increased to 150° C. After 16 h the solution was cooled to 60° C. and poured into water forming an off-white precipitate. The precipitate was separated by filtration and washed thoroughly with water, yielding 2.6 g of light brown powder (85% yield).

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후처리

  1. temperatureAfter 16 h the solution was cooled to 60° C.
  2. customThe precipitate was separated by filtration
  3. washwashed thoroughly with water

출처 및 근거

ORD 기록
ord-fcb9715acf1f47679face45236ef3d64
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315630B2

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