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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Furan → 1,4-Dihydro-1,4-epoxytriphenylene

HRID 871812
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인쇄 미리보기

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HRID 871812 반응식
Br[C:2]1[C:3]2[C:8]([C:9]3[CH:10]=[CH:11][CH:12]=[CH:13][C:14]=3[CH:15]=1)=[CH:7][CH:6]=[CH:5][CH:4]=2.[NH2-].[Na+].[O:18]1[CH:22]=[CH:21][CH:20]=[CH:19]1>C1COCC1>[O:18]1[CH:22]2[C:2]3[C:3]4[C:8]([C:9]5[C:14]([C:15]=3[CH:19]1[CH:20]=[CH:21]2)=[CH:13][CH:12]=[CH:11][CH:10]=5)=[CH:7][CH:6]=[CH:5][CH:4]=4
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8029FuranHCID 113099-BromophenanthreneHCID 24533Sodium amide

생성물 1

HCID 126679791,4-Dihydro-1,4-epoxytriphenylene

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
70 °C

실험 절차

9-Bromophenanthrene (18.6 g, 72.3 mmol), sodium amide (8.47 g, 217.0 mmol) were charged in a two-necked bottle. The bottle was then vacuumed and purged with nitrogen, and dried THF (120 mL) and furan (78.1 mL, 1.07 mmol) were added to the bottle. The mixture in the bottle was heated to 70° C. for reaction for 24 hours, and the resulting was filtered to remove metal. The filtrate was condensed to remove the solvent, and then purified by chromatography with hexanes to yield A (14.7 g, 83%) as white solid powder.

후처리

  1. additionwere added to the bottle
  2. filtrationthe resulting was filtered
  3. customto remove metal
  4. customcondensed
  5. customto remove the solvent
  6. custompurified by chromatography with hexanes
  7. customto yield A (14.7 g, 83%) as white solid powder

출처 및 근거

ORD 기록
ord-6b4fc6286bbf412f8523bb97a8254e73
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08974920B2

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