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

Nitric Acid → 5-Nitro-4,7-dimethyl-1,3-benzodioxole

HRID 1376554
노트
인쇄 미리보기

반응식

HRID 1376554 반응식
[N+:1]([O-:4])(O)=[O:2].[CH3:5][C:6]1[C:14]2[O:13][CH2:12][O:11][C:10]=2[C:9]([CH3:15])=[CH:8][CH:7]=1>CC(OCC1C2C(=CC=CC=2)C(COC(C)=O)=C2C=1C=CC=C2)=O.C(OC(=O)C)(=O)C>[N+:1]([C:8]1[CH:7]=[C:6]([CH3:5])[C:14]2[O:13][CH2:12][O:11][C:10]=2[C:9]=1[CH3:15])([O-:4])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 944Nitric AcidHCID 125809854,7-Dimethyl-1,3-benzodioxole

생성물 1

HCID 218404755-Nitro-4,7-dimethyl-1,3-benzodioxole

시약·촉매·용매 2

HCID 7918Acetic Anhydride용매HCID 613145Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester용매

실험 절차

A solution of 0.92 mL of concentrated nitric acid in 17 mL of acetic arthydride is added dropwise to a stirred solution of 2.20 g of 4,7-dimethyl-1,3-benzodioxole in 60 mL of acetic anhydride at -5° C. After 30 minutes, the mixture is poured over 100 g of crushed ice and allowed to stir for 30 minutes as a white precipitate falls out of solution. The solid is filtered, taken up in ether, dried over magnesium sulfate and concentrated under reduced pressure to afford 2.1 g of 5-nitro-4,7-dimethyl-1,3-benzodioxole.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. filtrationThe solid is filtered
  2. dry with materialdried over magnesium sulfate
  3. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-c4649a188f544ee48bbdcd0d15e73bf3
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05663189

반응 노트

불러오는 중…