Water → 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one

HRID 1452463노트

반응식

HRID 1452463 반응식
F[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[CH2:7][CH2:6][CH2:5]2.[C:13]1([SH:19])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O-])([O-])=O.[K+].[K+].O>CN1C(=O)CCC1.CCOC(C)=O>[C:13]1([S:19][C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[C:8](=[O:12])[CH2:7][CH2:6][CH2:5]3)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

7

반응 조건

온도
80 °C

실험 절차

A solution of 6-fluoro-3,4-dihydro-2H-naphthalen-1-one (5.51 g, 33.56 mmol), benzenethiol (4.07 g, 3.79 mL, 36.92 mmol) and K2CO3 (9.28 g, 67.12 mmol) in 50 mL of N-methyl pyrrolidinone (NMP) was heated to 80° C. under argon and stirred at 80° C. for 2 hours. The reaction mixture was poured int 500 mL of water and diluted with 300 mL of EtOAc. The layers were separated and the aqueous layer was extracted twice with 250 mL of EtOAc. The combinded organic layers were washed with water, saturated brine, and then dried over MgSO4. The solvent was removed under reduced pressure to yield an oil which was eluted through silica gel using hexanes/EtOAc (9:1). Removal of solvent under reduced pressure provided 8.05 g (31.65 mmol, 94.31%) of 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one as a pale yellow oil. MS: 255 (M+H)+.

후처리

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted twice with 250 mL of EtOAc
  3. washThe combinded organic layers were washed with water, saturated brine
  4. dry with materialdried over MgSO4
  5. customThe solvent was removed under reduced pressure
  6. customto yield an oil which
  7. washwas eluted through silica gel
  8. customRemoval of solvent under reduced pressure

출처 및 근거

ORD 기록
ord-8193b0c616434da28a24de83ddfa005d
출처 데이터셋
uspto-grants-2009_01
특허 번호
US07473690B2

반응 노트

불러오는 중…