반응식
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([CH:11]=O)=[CH:8][CH:9]=2)[N:4]=[CH:3][CH:2]=1.[Br-].[O:14]1CCO[CH:15]1[CH2:19][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.COCCOCCN(CCOCCOC)CCOCCOC>ClCCl.C([O-])([O-])=O.[K+].[K+]>[N:1]1[C:10]2[C:5](=[CH:6][C:7](/[CH:11]=[CH:19]/[CH:15]=[O:14])=[CH:8][CH:9]=2)[N:4]=[CH:3][CH:2]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of 6-quinoxalinecarboxaldehyde (0.62 g, 3.92 mmol, prepared as described in Photochem. Photobiol. 1991, 54, 7), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (2.50 g, 5.82 mmol), and TDA-1 (1.20 mL, 3.75 mmol) in dichloromethane (20 mL) and sat. aq. K2CO3 (20 mL) was heated to reflux for 4 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×20 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (Na2SO4), and concentrated. THF (10 mL) and 10% HCl (10 mL) were added and the mixture was stirred for 1 h at rt. The mixture was cooled to 0° C., the precipitated solids were removed by filtration, washed with water and dried in vacuo to give 0.47 g (65%) of the title compound as a tan solid. MS 185 (M+H)+.
후처리
- temperaturewas heated
- temperatureto reflux for 4 h
- customThe layers were separated
- extractionthe aqueous layer was extracted with dichloromethane (2×20 mL)
- washThe combined organic layers were washed with water (50 mL) and brine (50 mL)
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- additionTHF (10 mL) and 10% HCl (10 mL) were added
- temperatureThe mixture was cooled to 0° C.
- customthe precipitated solids were removed by filtration
- washwashed with water
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-d7424d04e2f24310a1dbd88da33e8436
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06713455B2
연결된 노트
불러오는 중…