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

5-Nitro-6-bromo-1h,3h-benzo[de]isochromene → 5-Nitro-1,3-dihydrobenzo[de]isochromene-6-carbonitrile

HRID 217285
노트
인쇄 미리보기

반응식

HRID 217285 반응식
[N+:1]([C:4]1[C:5](Br)=[C:6]2[CH:15]=[CH:14][CH:13]=[C:12]3[C:7]2=[C:8]([CH:16]=1)[CH2:9][O:10][CH2:11]3)([O-:3])=[O:2].[Cu][C:19]#[N:20]>CN(C=O)C>[N+:1]([C:4]1[C:5]([C:19]#[N:20])=[C:6]2[CH:15]=[CH:14][CH:13]=[C:12]3[C:7]2=[C:8]([CH:16]=1)[CH2:9][O:10][CH2:11]3)([O-:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 578987455-Nitro-6-bromo-1h,3h-benzo[de]isochromeneHCID 178418546HCID 178418546, 화합물

생성물 1

HCID 578986665-Nitro-1,3-dihydrobenzo[de]isochromene-6-carbonitrile

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
140 °C

실험 절차

5-Nitro-6-bromo-1H,3H-benzo[de]isochromene (23.0 g, 78.2 mmol) was dissolved in anhydrous DMF (500 mL). Then, copper (I) cyanide (10.5 g, 117 mmol) was added to the mixture at room temperature. The mixture was stirred at the internal temperature of 140° C. for 3 hours, and then cooled to 70° C. The resulting insoluble material was separated by filtration. The filtrate was poured into water (1500 mL), and stirred at room temperature for 2 hours. The resulting precipitate was collected by filtration, washed with acetonitrile, and air-dried. The title compound was obtained as yellow solid (15.9 g, 85%).

후처리

  1. temperaturecooled to 70° C
  2. customThe resulting insoluble material was separated by filtration
  3. additionThe filtrate was poured into water (1500 mL)
  4. stirringstirred at room temperature for 2 hours
  5. filtrationThe resulting precipitate was collected by filtration
  6. washwashed with acetonitrile
  7. customair-dried

출처 및 근거

ORD 기록
ord-216c678032994032a92faa91f22a2592
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08193351B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트