Hydrochloric Acid → 3-((2,4,6-Trichloro-N-methylphenylsulfonamido)methoxy)propionic Acid

HRID 424626

반응식

HRID 424626 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

6

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

  1. additionwere added
  2. customThe phases were separated
  3. washthe organic phase was washed with water (3×20 ml) and saturated sodium chloride solution (2×20 ml)
  4. dry with materialdried with Na2SO4
  5. concentrationconcentrated i
  6. extraction(30 ml) and the mixture was extracted with EtOAc (3×20 ml)
  7. extractionextracted with EtOAc (3×20 ml)
  8. washThe combined organic phases were washed with water (3×20 ml) and saturated sodium chloride solution (2×20 ml)
  9. dry with materialdried with Na2SO4
  10. concentrationconcentrated i

출처 및 근거

ORD 기록
ord-96dbd91ff27e48d4808e4acf0708f032
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08106055B2

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