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

Sodium Hydroxide → 3-Methoxy-2-methylbenzonitrile

HRID 1107715
노트
인쇄 미리보기

반응식

HRID 1107715 반응식
Cl.[NH2:2]O.[CH3:4][O:5][C:6]1[C:7]([CH3:14])=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH:9]=O.[OH-].[Na+]>C(O)=O>[CH3:4][O:5][C:6]1[C:7]([CH3:14])=[C:8]([CH:11]=[CH:12][CH:13]=1)[C:9]#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 131626633-Methoxy-2-methylbenzaldehyde

생성물 1

HCID 110947703-Methoxy-2-methylbenzonitrile수율 80%

시약·촉매·용매 1

HCID 284Formic Acid용매

실험 절차

Hydroxylamine hydrochloride (0.75 g, 11 mmol) was added to 3-methoxy-2-methylbenzaldehyde (1.25 g, 8.32 mmol) in formic acid (89-91%) (10 ml), and the mixture heated to reflux for 40 min., cooled, diluted with ice-cold water, basified with 10% aqueous sodium hydroxide solution and extracted with diethyl ether. The organic extract was washed with saturated aqueous sodium chloride (50 ml), dried over magnesium sulphate and evaporated. The residue was purified by flash chromatography over silica gel eluting with 5% diethyl ether in hexane to afford the product as a white solid (0.98 g). M+ 147; 360 MHz 1H n.m.r (CDCl3) 7.26-7.17 (2H, m), 7.02 (1H, d, J 7.9 Hz), 3.86 (3H, s), 2.41 (3H, s).

후처리

  1. temperaturethe mixture heated
  2. temperatureto reflux for 40 min.
  3. temperaturecooled
  4. additiondiluted with ice-cold water
  5. extractionextracted with diethyl ether
  6. extractionThe organic extract
  7. washwas washed with saturated aqueous sodium chloride (50 ml)
  8. dry with materialdried over magnesium sulphate
  9. customevaporated
  10. customThe residue was purified by flash chromatography over silica gel eluting with 5% diethyl ether in hexane

출처 및 근거

ORD 기록
ord-9f70d035c6c641d08f2557ab721148a2
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06063789

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트