반응식
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([OH:13])=[CH:5][CH:4]=1.C[C:15](OI(OC(C)=O)C1C=CC=CC=1)=[O:16].C([O-])(O)=O.[Na+]>>[CH3:1][O:2][C:3]1([O:16][CH3:15])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](=[O:13])[CH:5]=[CH:4]1참가 물질
실험 절차
A solution of 4-methoxy-1-naphthol (2.76 g, 15.8 mmol) and DAIB (6.10 g, 18.9 mmol) on methanol (75 mL) was stirred at 25° C. under a nitrogen atmosphere for 1 h. The resultant dark blue solution was poured into a saturated NaHCO3 (aq) solution (75 mL), then the mixture concentrated to approx. 50 mL in vacuo. The blue oil was extracted with dichloromethane (3×75 mL) and the organic layer washed with water (2×75 mL) and brine (2×75 mL), then dried (MgSO4), filtered and concentrated in vacuo (water bath temperature <40° C.) to yield 4,4-dimethoxy-4H-naphthalen-1-one as a dark-blue semi-solid which was used without further purification; 1H NMR (CDCl3) δ 8.15 (1H, d, J 8.0 Hz, ArH), 7.40–7.85 (3H, m, ArH), 6.90 (1H, d, J 12.2 Hz, H-3), 6.55 (1H, d, J 12.2 Hz, H-2), 3.15 (6H, s, OCH3).
후처리
- concentrationthe mixture concentrated to approx. 50 mL in vacuo
- extractionThe blue oil was extracted with dichloromethane (3×75 mL)
- washthe organic layer washed with water (2×75 mL) and brine (2×75 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo (water bath temperature <40° C.)
출처 및 근거
- ORD 기록
- ord-86ec5291c9694b74bed5ac9fe40de5b1
- 출처 데이터셋
- uspto-grants-2006_12
- 특허 번호
- US07144893B2
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