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2-Methylbenzoxazole → 2-(Benzo[d]oxazol-2-yl)-N,N-dimethylethenamine

HRID 868917
노트
인쇄 미리보기

반응식

HRID 868917 반응식
[CH3:1][C:2]1[O:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.C[C:12]([N:14]([CH3:16])[CH3:15])=O>CN(C=O)C>[O:3]1[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=[C:2]1/[CH:1]=[CH:12]/[N:14]([CH3:16])[CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 72252-MethylbenzoxazoleHCID 31374Dimethylacetamide

생성물 1

HCID 149729932-(Benzo[d]oxazol-2-yl)-N,N-dimethylethenamine수율 51.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
145 °C

실험 절차

A mixture of 2-methylbenzo[d]oxazole (3 g, 22.6 mmol) in DMF (3.2 g) and dimethyl acetamide (3.5 g, 29.3 mmol) was stirred under N2 at 145° C. overnight. Then the solution was poured into ice-water and extracted with EtOAc (100 mL×2). The organic phase was washed, dried and concentrated. The residue was purified by column chromatography to get the title compound (2.2 g). MS (ESI) m/z 134 (M+H+).

후처리

  1. extractionextracted with EtOAc (100 mL×2)
  2. washThe organic phase was washed
  3. customdried
  4. concentrationconcentrated
  5. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-8751eac5577644d588bc9396371a866f
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969349B2

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