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Hydrochloric Acid → HCID 53862169, 화합물

HRID 1776475
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인쇄 미리보기

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HRID 1776475 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])([O-:3])=[O:2].C([O-])([O-])=O.[K+].[K+].Br[CH2:18][CH:19]1[CH2:21][CH2:20]1.Cl>CC#N.CCOC(C)=O>[CH:19]1([CH2:18][O:10][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N+:1]([O-:3])=[O:2])[CH2:21][CH2:20]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 69472-NitrophenolHCID 11430Potassium CarbonateHCID 81503Bromomethylcyclopropane

생성물 1

HCID 53862169HCID 53862169, 화합물수율 97%

시약·촉매·용매 2

HCID 6342Acetonitrile용매

반응 조건

온도
85 °C

실험 절차

A mixture of 2-nitrophenol (1 g, 7.19 mmol), K2CO3 (1.192 g, 8.63 mmol), and (bromomethyl)cyclopropane (0.837 ml, 8.63 mmol) in CH3CN (40 ml) was heated to 85° C. overnight. The mixture was portioned between EtOAc and HCl 1N. The organic phase was dried over Na2SO4 and the solvent was removed. 1-(cyclopropylmethoxy)-2-nitrobenzene was obtained as a crude (1.352 g, 7.00 mmol, 97% yield) and used in the next step without further purification.

후처리

  1. dry with materialThe organic phase was dried over Na2SO4
  2. customthe solvent was removed

출처 및 근거

ORD 기록
ord-f5eb709722784993b97f929057f8ce12
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09265768B2

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 8857
Ethyl Acetate
용매