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Methyl iodide → 8-Fluoro-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one

HRID 1723292
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HRID 1723292 반응식
[H-].[Na+].[F:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:16]=1[NH:15][C:14]1[CH2:13][CH2:12][CH2:11][C:10](=[O:17])[C:9]2=1.[CH3:18]I>C1COCC1.[Cl-].[Na+].O>[F:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:16]=1[N:15]([CH3:18])[C:14]1[CH2:13][CH2:12][CH2:11][C:10](=[O:17])[C:9]2=1
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참가 물질

6

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 221477458-Fluoro-1,2,3,9-tetrahydro-4H-carbazol-4-one

생성물 1

HCID 197698468-Fluoro-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회HCID 57417360Sodium chloride; water
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용매

실험 절차

To a suspension of sodium hydride (80% dispersion in oi; 1.15 g) in dry THF (50 ml) under nitrogen was added 8-fluoro-1,2,3,9-tetrahydro-4H-carbazol-4-one (6.5 g) in dry THF (50 ml), and the mixture was stirred for 1 h. Methyl iodide (4.1 ml) was added, and the mixture was stirred for 3 h. The mixture was then poured into brine (300 ml) and extracted with ether (2×300 ml). The combined, dried organic extracts were evaporated in vacuo to give the title compound (5.77 g), m.p. 126°-128°.

후처리

  1. stirringthe mixture was stirred for 3 h
  2. extractionextracted with ether (2×300 ml)
  3. customdried organic extracts were evaporated in vacuo

출처 및 근거

ORD 기록
ord-5bf49a29b90847588715af145ac30855
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04859662

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