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Dichloromethane → 2,3-Dihydrobenzofuran-5-carboxaldehyde

HRID 324605
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HRID 324605 반응식
ClCCl.[O:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[CH2:6][CH2:5]1.[CH3:13][O:14]C(Cl)Cl>[Cl-].[Ti+4].[Cl-].[Cl-].[Cl-].O>[O:4]1[C:8]2[CH:9]=[CH:10][C:11]([CH:13]=[O:14])=[CH:12][C:7]=2[CH2:6][CH2:5]1
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참가 물질

6

반응물 3

HCID 6344DichloromethaneHCID 10329DihydrobenzofuranHCID 21004Methane, dichloromethoxy-

생성물 1

HCID 7359012,3-Dihydrobenzofuran-5-carboxaldehyde수율 61,555.602%

시약·촉매·용매 2

HCID 160960Diamminetetrachlorotitanate(IV)촉매HCID 962Water용매

실험 절차

Titanium chloride (28 ml) was dropwise added to a dichloromethane (100 ml) solution containing 2,3-dihydrobenzofuran (10.0 g, 83.2 mmols) and dichloromethyl methyl ether (11.3 ml, 0.125 mmols), while cooling with ice. The mixture was stirred for 1 hour, while still cooling with ice, and then water was added thereto. Dichloromethane was removed under reduced pressure, and the residue was extracted with ethyl acetate. The extract was washed with a saturated saline solution, then dried with anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified through silica-gel chromatography (hexane/ethyl acetate=1/1) to obtain 11.4 g (yield: 92%) of the target compound. This was oily.

후처리

  1. temperaturewhile cooling with ice
  2. temperaturewhile still cooling with ice
  3. customDichloromethane was removed under reduced pressure
  4. extractionthe residue was extracted with ethyl acetate
  5. washThe extract was washed with a saturated saline solution
  6. dry with materialdried with anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified through silica-gel chromatography (hexane/ethyl acetate=1/1)

출처 및 근거

ORD 기록
ord-e60d3f4560d94190a849d10d23a90938
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06218429B1

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