반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[S:10]([N:13]([CH2:15][O:16][CH2:17][CH2:18][CH2:19][OH:20])[CH3:14])(=[O:12])=[O:11].C(OI(C1C=CC=CC=1)OC(=O)C)(=[O:23])C.Cl.CCOC(C)=O>C(#N)C.O>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[S:10]([N:13]([CH2:15][O:16][CH2:17][CH2:18][C:19]([OH:23])=[O:20])[CH3:14])(=[O:11])=[O:12]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
2,4,6-Trichloro-N-(3-hydroxypropoxymethyl)-N-methylbenzenesulfonamide (363 mg, 1 mmol), 2,2,6,6-tetramethylpiperidin-1-yloxy radical (38 mg, 0.245 mmol) and [bis(acetoxy)iodo]benzene (705 mg, 2.19 mmol) were dissolved in acetonitrile/water (1:1; 8 ml) and the solution was stirred at RT for 30 min. The reaction soln. was then cooled with ice, and 2 N hydrochloric acid (4 ml) and EtOAc (40 ml) were added. The phases were separated and the organic phase was washed with water (3×20 ml) and saturated sodium chloride solution (2×20 ml), dried with Na2SO4 and concentrated i. vac. The compound was taken up in 1 N sodium carbonate soln. (30 ml) and the mixture was extracted with EtOAc (3×20 ml). The aqueous phase was then adjusted to pH 3 with 2 N hydrochloric acid and extracted with EtOAc (3×20 ml). The combined organic phases were washed with water (3×20 ml) and saturated sodium chloride solution (2×20 ml), dried with Na2SO4 and concentrated i. vac. Yield: 310 mg (82%)
후처리
- additionwere added
- customThe phases were separated
- washthe organic phase was washed with water (3×20 ml) and saturated sodium chloride solution (2×20 ml)
- dry with materialdried with Na2SO4
- concentrationconcentrated i
- extraction(30 ml) and the mixture was extracted with EtOAc (3×20 ml)
- extractionextracted with EtOAc (3×20 ml)
- washThe combined organic phases were washed with water (3×20 ml) and saturated sodium chloride solution (2×20 ml)
- dry with materialdried with Na2SO4
- concentrationconcentrated i
출처 및 근거
- ORD 기록
- ord-96dbd91ff27e48d4808e4acf0708f032
- 출처 데이터셋
- uspto-grants-2012_01
- 특허 번호
- US08106055B2
연결된 노트
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