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Methane, dichloromethoxy- → HCID 19047057, 화합물

HRID 1780615
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HRID 1780615 반응식
[CH3:1][C:2]1([CH3:14])[CH2:6][C:5]2[C:7]([CH3:13])=[C:8]([CH3:12])[CH:9]=[C:10]([CH3:11])[C:4]=2[O:3]1.[CH3:15][O:16]C(Cl)Cl>ClCCl.[Cl-].[Ti+4].[Cl-].[Cl-].[Cl-]>[CH3:1][C:2]1([CH3:14])[CH2:6][C:5]2[C:7]([CH3:13])=[C:8]([CH3:12])[C:9]([CH:15]=[O:16])=[C:10]([CH3:11])[C:4]=2[O:3]1
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참가 물질

5

반응물 2

HCID 21004Methane, dichloromethoxy-HCID 19047070HCID 19047070, 화합물

생성물 1

HCID 19047057HCID 19047057, 화합물

시약·촉매·용매 2

HCID 160960Diamminetetrachlorotitanate(IV)촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of 34.5 g of the 2,3-dihydro-2,2,4,5,7-pentamethylbenzofuran in 200 ml of absolute dichloromethane was added 200 ml of titanium chloride (IV) and 18 ml of α,α-dichloromethyl methyl ether at 0° C. With stirring at room temperature for 45 minutes and refluxing for 15 minutes, the reaction mixture was quenched with 300 ml of water and the aqueous layer was extracted with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford a crude product. Final purification was carried by recrystallization to afford 37.2 g of 2,3-dihydro-2,2,4,5,7-pentamethyl-benzofuran-6-carboxaldehyde as a white solid.

후처리

  1. temperaturerefluxing for 15 minutes
  2. customthe reaction mixture was quenched with 300 ml of water
  3. extractionthe aqueous layer was extracted with dichloromethane
  4. dry with materialThe combined organic extracts were dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customto afford a crude product
  8. customFinal purification
  9. customwas carried by recrystallization

출처 및 근거

ORD 기록
ord-28b53685327d4b428ca714f85bce3f76
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05631208

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