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Diethyl Ether → HCID 22237792, 화합물

HRID 1975897
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HRID 1975897 반응식
[CH3:1][C:2]1[C:3]([CH3:12])([CH3:11])[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[C:13]([O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][I:22])(=[O:15])[CH3:14].CCOCC>ClC1C=CC=CC=1Cl>[I-:22].[CH3:1][C:2]1[C:3]([CH3:12])([CH3:11])[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N+:6]=1[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][O:16][C:13]([CH3:14])=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 154273H-Indole, 2,3,3-trimethyl-HCID 10988867HCID 10988867, 화합물

생성물 1

HCID 22237792HCID 22237792, 화합물

시약·촉매·용매 1

HCID 72391,2-Dichlorobenzene용매

반응 조건

온도
120 °C

실험 절차

A mixture of 2,3,3-trimethyl-3H-benzo[b]azole (2.39 g, 15 mmol) and 5-iodopentyl acetate (3.84 g, 15 mmol) in 1,2-dichlorobenzene (15 ml) were heated at 120° C. for 6 h and then cooled to ambient temperature. The mixture was then dripped into Et2O which precipitated the title compound as a red gum which was collected and used without any further purification in subsequent reactions.

후처리

  1. temperaturecooled to ambient temperature
  2. customprecipitated the title compound as a red gum which
  3. customwas collected
  4. customused without any further purification in subsequent reactions

출처 및 근거

ORD 기록
ord-b2c17977f2274bc682c2742ccb29f7d7
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06225050B1

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