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

Nitric Acid → 2-Cyano-5-nitroindane

HRID 1708558
노트
인쇄 미리보기

반응식

HRID 1708558 반응식
[N+:1]([O-:4])(O)=[O:2].[C:5]([CH:7]1[CH2:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH2:8]1)#[N:6]>C(OC(=O)C)(=O)C>[C:5]([CH:7]1[CH2:15][C:14]2[C:9](=[CH:10][CH:11]=[C:12]([N+:1]([O-:4])=[O:2])[CH:13]=2)[CH2:8]1)#[N:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 232396182,3-Dihydro-1H-indene-2-carbonitrile

생성물 1

HCID 189589622-Cyano-5-nitroindane수율 81%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

Fuming nitric acid (40 ml, 1.5 g/ml) was added dropwise with stirring to acetic anhydride (80 ml ) keeping the temperature of the mixture at 0° C. After the addition was complete 2-cyanoindane (11.33 g, 79.5 mmol), (J. Chem. Soc. (B), (1969), 1197) was added dropwise with stirring over 30 minutes maintaining the reaction temperature between -5° and 0° C. The mixture was stirred for a further 15 minutes then poured onto ice. The mixture was extracted with dichloromethane (4×150 ml) and the extracts were washed with saturated aqueous sodium bicarbonate (3×150 ml), dried over magnesium sulphate and the solvent evaporated under reduced pressure. The residue was recrystallised from ethanol to give 2-cyano-5-nitroindane (12.09 g, 81%) as a yellow solid, m.p. 80°-82° C.

후처리

  1. customat 0° C
  2. additionAfter the addition
  3. additionwas added dropwise
  4. temperaturemaintaining the reaction temperature between -5° and 0° C
  5. stirringThe mixture was stirred for a further 15 minutes
  6. additionthen poured onto ice
  7. extractionThe mixture was extracted with dichloromethane (4×150 ml)
  8. washthe extracts were washed with saturated aqueous sodium bicarbonate (3×150 ml)
  9. dry with materialdried over magnesium sulphate
  10. customthe solvent evaporated under reduced pressure
  11. customThe residue was recrystallised from ethanol

출처 및 근거

ORD 기록
ord-d98ba50076f94851a87b012e7c1c7191
출처 데이터셋
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05358953

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트