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

Nitric Acid → HCID 19762126, 화합물

HRID 248796
노트
인쇄 미리보기

반응식

HRID 248796 반응식
[CH2:1]([O:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=[CH:10][CH:9]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[N+:21]([O-])([OH:23])=[O:22]>C(OC(=O)C)(=O)C.CCCCCC>[CH2:15]([O:14][C:11]1[CH:12]=[CH:13][C:8]([O:7][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])=[CH:9][C:10]=1[N+:21]([O-:23])=[O:22])[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 944Nitric AcidHCID 43511781,4-dihexyloxybenzene

생성물 1

HCID 19762126HCID 19762126, 화합물수율 97%

시약·촉매·용매 2

HCID 7918Acetic Anhydride용매HCID 8058Hexane용매

실험 절차

11.6 g of 1,4-di(n-hexyloxy)benzene was dissolved in a mixed solvent of 50 ml of acetic anhydride and 50 ml of n-hexane, and 4 ml of concentrated nitric acid having a specific gravity of 1.42 was dropwise added thereto at a room temperature of 20° C. over 3 minutes. The internal temperature rose to 46° C., and the reaction was completed to obtain 13.1 g of 2,5-di(n-hexyloxy)nitrobenzene (yield: 97%).

후처리

  1. additionwas dropwise added
  2. customrose to 46° C.

출처 및 근거

ORD 기록
ord-ff9ad8b41ab449eeac468c0d2151c7d6
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05212042

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트