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1,3-Dibromopropane → 6-(3-Bromopropoxy)-3-methyl-1-benzofuran

HRID 2235873
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HRID 2235873 반응식
[CH3:1][C:2]1[C:6]2[CH:7]=[CH:8][C:9]([OH:11])=[CH:10][C:5]=2[O:4][CH:3]=1.[Br:12][CH2:13][CH2:14][CH2:15]Br>[OH-].[Na+]>[Br:12][CH2:13][CH2:14][CH2:15][O:11][C:9]1[CH:8]=[CH:7][C:6]2[C:2]([CH3:1])=[CH:3][O:4][C:5]=2[CH:10]=1
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참가 물질

4

반응물 2

HCID 80011,3-DibromopropaneHCID 108556243-Methyl-6-hydroxybenzofuran

생성물 1

HCID 593004356-(3-Bromopropoxy)-3-methyl-1-benzofuran수율 169.6%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매2회

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온도
80 °C

실험 절차

To a solution of 3-methyl-1-benzofuran-6-ol (0.20 g, 1.35 mmol) in NaOH (6 M aqueous solution, 0.25 mL) was added 1,3-dibromopropane (0.48 mL, 0.46 mmol), and the mixture was heated at 80° C. for 2 h. The reaction mixture was cooled to rt, and NaOH (6 M aqueous solution, 0.11 mL) was added. The reaction mixture was heated at 80° C. for 1 h, cooled to rt, and partitioned between CH2Cl2 and NaHCO3 (saturated aqueous solution). The organic layer was dried, filtered, concentrated under reduced pressure, and purified by silica gel column chromatography (EtOAc/hexane (v/v)=1:19) to give 210 mg (58%) of the title compound containing minor impurities. This material was used in next step without further purification. 1H NMR (300 MHz, CDCl3): δ 7.38 (d, 1H), 7.32 (s, 1H), 7.0 (s, 1H), 6.88 (dd, 1H), 4.14 (t, 2H), 3.62 (t, 2H), 2.40-2.28 (m, 2H), 2.20 (s, 3).

후처리

  1. temperatureThe reaction mixture was cooled to rt
  2. temperatureThe reaction mixture was heated at 80° C. for 1 h
  3. temperaturecooled to rt
  4. custompartitioned between CH2Cl2 and NaHCO3 (saturated aqueous solution)
  5. customThe organic layer was dried
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. custompurified by silica gel column chromatography (EtOAc/hexane (v/v)=1:19)

출처 및 근거

ORD 기록
ord-ebf929ad36364908a89205677f5736aa
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07714004B2

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