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HCID 23206558, 화합물 → HCID 23206535, 화합물

HRID 1289426
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HRID 1289426 반응식
[CH2:1]([O:3][P:4]([CH:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([C:19]([F:22])([F:21])[F:20])[CH:15]=2)[N:10]1C(OCC(Cl)(Cl)Cl)=O)(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2]>CO.[Zn]>[CH2:6]([O:5][P:4]([CH:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([C:19]([F:20])([F:21])[F:22])[CH:15]=2)[NH:10]1)(=[O:8])[O:3][CH2:1][CH3:2])[CH3:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 23206558HCID 23206558, 화합물

생성물 1

HCID 23206535HCID 23206535, 화합물

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 887Methanol용매

반응 조건

온도
90 °C

실험 절차

15.4 g of 1-(2,2,2-trichloroethoxycarbonyl)-6-trifluoromethyl-1,2,3,4-tetrahydroquinoline-2-phosphonic acid diethyl ester is dissolved in 400 ml of methanol, mixed with 7.2 g of zinc powder and stirred under nitrogen for 1.5 hours at 90° C. It is filtered on diatomaceous earth and the filtrate is concentrated by evaporation. The crude product is purified by column chromatography and recrystallized from isopropyl ether.

후처리

  1. filtrationIt is filtered on diatomaceous earth
  2. concentrationthe filtrate is concentrated by evaporation
  3. customThe crude product is purified by column chromatography
  4. customrecrystallized from isopropyl ether

출처 및 근거

ORD 기록
ord-285dce98428d439d8159351dd7b02540
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750526

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