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Calcium Carbonate → 1,4-Dimethoxy-3-bromo-2-hydroxymethylnaphthalene

HRID 1527702
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HRID 1527702 반응식
[Br:1][C:2]1[C:11]([CH2:12]Br)=[C:10]([O:14][CH3:15])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]=1[O:16][CH3:17].C([O-])([O-])=[O:19].[Ca+2]>COCCOC.O>[Br:1][C:2]1[C:11]([CH2:12][OH:19])=[C:10]([O:14][CH3:15])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]=1[O:16][CH3:17]
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참가 물질

5

반응물 2

HCID 10112Calcium CarbonateHCID 104061942-Bromo-3-bromomethyl-1,4-dimethoxynaphthalene

생성물 1

HCID 105180901,4-Dimethoxy-3-bromo-2-hydroxymethylnaphthalene수율 105%

시약·촉매·용매 2

HCID 962Water용매HCID 80711,2-Dimethoxyethane용매

실험 절차

Following a modified procedure of Smith et al.,25 dibromide 36 (1.73 g, 4.80 mmol) was dissolved in 1,2-dimethoxyethane (50.0 mL), and then added to CaCO3 (2.50 g, 25.0 mmol) in H2O (50.0 mL) at room temperature. The reaction was heated under reflux for TIME and then cooled to room temperature. The reaction was extracted with EtOAc (75.0 mL), and the organic layers are washed with brine. The organic layer was dried over MgSO4 and filtered. The resulting pink solid was then purified by flash column chromatography (1:3 EtOAc:hexanes) to provide 37 (1.49 g, 5.01 mmol, 105%) as a pink solid.

후처리

  1. temperatureThe reaction was heated
  2. temperatureunder reflux for TIME
  3. extractionThe reaction was extracted with EtOAc (75.0 mL)
  4. washthe organic layers are washed with brine
  5. dry with materialThe organic layer was dried over MgSO4
  6. filtrationfiltered
  7. customThe resulting pink solid was then purified by flash column chromatography (1:3 EtOAc:hexanes)

출처 및 근거

ORD 기록
ord-e2499e625e1f4e70b1aa8ea0966629e4
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09089605B2

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