홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Isopropanol → 6-Methyl-5-nitropicolinic acid

HRID 514844
노트
인쇄 미리보기

반응식

HRID 514844 반응식
[CH3:1][C:2]1[N:7]=C(C#N)[CH:5]=[CH:4][C:3]=1[N+:10]([O-:12])=[O:11].C[C:14]([CH3:17])([O-:16])C.[K+].CC([OH:22])C>O>[CH3:1][C:2]1[N:7]=[C:17]([C:14]([OH:22])=[O:16])[CH:5]=[CH:4][C:3]=1[N+:10]([O-:12])=[O:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 124040386-Methyl-5-nitropyridine-2-carbonitrileHCID 23665647Potassium tert-butoxide

생성물 1

HCID 74720376-Methyl-5-nitropicolinic acid

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
100 °C

실험 절차

To a solution of 6-methyl-5-nitropicolinonitrile (31B, 500 mg, 3.1 mmol) in 2-propanol (1 mL) and water (5 mL) was added potassium tert-butoxide (687 mg, 6.13 mmol). The mixture was stirred at 100° C. overnight, when LCMS indicated that the reaction was complete. The mixture diluted with water, and then extracted with DCM (10 mL×3). The aqueous phase was acidified with 1N HCl solution, and extracted with DCM. The organic layer was dried and concentrated to give the crude product which was used to the next step without further purification. LC-MS: m/z 181 (M−H)+

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. extractionextracted with DCM (10 mL×3)
  2. extractionextracted with DCM
  3. customThe organic layer was dried
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-47c974a660c04eada2cd88c82e58cdfb
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108921B2

반응 노트

불러오는 중…