Methane, dichloromethoxy- → 4-Fluoro-1-methoxy-2-naphthaldehyde

HRID 2075538노트

반응식

HRID 2075538 반응식
[CH3:1][O:2][CH:3](Cl)Cl.[Sn](Cl)(Cl)(Cl)Cl.[F:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:15]([O:22]C)=[CH:14][CH:13]=1>ClCCl>[F:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:3]([O:2][CH3:1])=[C:14]([CH:15]=[O:22])[CH:13]=1

참가 물질

5

반응 조건

온도
5 °C

실험 절차

5.25 mL of dichloromethyl methyl ether were dissolved in 40 mL dichloromethane and cooled to +5° C. 6.75 mL tin(IV) chloride were added neat over 45 min to the solution. After the addition the mixture was stirred for 45 min at 5° C. 11.4 g 4-fluoro-1-methoxy-naphthalene in 30 mL dichloromethane was added over 1 h. Then the cooling bath was removed, and the mixture was stirred for 2 h at ambient temperature. It was then poured into ice/water. The dichloromethane layer was separated and the aqueous phase was extracted with dichloromethane. The combined dichloromethane layers were washed with water, dried over sodium sulfate, filtered through celite and concentrated in vacuo. The residue was treated with pentane to yield 9.3 g of 4-fluoro-1-methoxynaphthalene-2-carbaldehyde as a brown solid.

후처리

  1. temperaturecooled to +5° C
  2. additionAfter the addition the mixture
  3. customThen the cooling bath was removed
  4. stirringthe mixture was stirred for 2 h at ambient temperature
  5. additionIt was then poured into ice/water
  6. customThe dichloromethane layer was separated
  7. extractionthe aqueous phase was extracted with dichloromethane
  8. washThe combined dichloromethane layers were washed with water
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered through celite and
  11. concentrationconcentrated in vacuo
  12. additionThe residue was treated with pentane

출처 및 근거

ORD 기록
ord-22b516aac7db4383992fbdb642e42c7c
출처 데이터셋
uspto-grants-2011_04
특허 번호
US07919628B2

반응 노트

불러오는 중…