Ammonium Chloride → 2-Amino-5-(benzyloxy)benzenesulfonamide

HRID 2224765노트

반응식

HRID 2224765 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([N+:19]([O-])=O)=[C:13]([S:15]([NH2:18])(=[O:17])=[O:16])[CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl-].[NH4+]>CO.O.[Fe]>[NH2:19][C:12]1[CH:11]=[CH:10][C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:14][C:13]=1[S:15]([NH2:18])(=[O:16])=[O:17]

참가 물질

6

반응물 2

HCID 25517Ammonium ChlorideHCID 670638975-(Benzyloxy)-2-nitrobenzenesulfonamide

생성물 1

HCID 670639862-Amino-5-(benzyloxy)benzenesulfonamide수율 97.1%

시약·촉매·용매 3

HCID 23925Iron촉매HCID 887Methanol용매HCID 962Water용매

실험 절차

A suspension of the product of Example 2C (7.26 g, 23.57 mmol), ammonium chloride (8.27 g, 155 mmol), and iron powder (8.11 g, 145 mmol) in methanol (188 mL) and water (94 mL) was stirred at reflux for 2 hours. The mixture was filtered while hot through celite®, and the filter cake was washed with hot methanol (200 mL). The filtrate was concentrated to an approximate volume of 100 mL and then extracted with ethyl acetate (400 mL). The organic layer was washed with water and saturated sodium chloride solution, dried (Na2SO4), filtered through celite® and concentrated in vacuo to afford the title compound (6.37 g, 97%). 1H NMR (300 MHz, DMSO-d6): δ 7.38 (m, 7 H), 7.22 (m, 2 H), 7.01 (dd, J=8.82, 2.94 Hz, 1 H), 6.76 (d, J=8.82 Hz, 1 H), 5.46 (s, 2 H), 4.98 (s, 2 H).

후처리

  1. temperatureat reflux for 2 hours
  2. filtrationThe mixture was filtered while hot through celite®
  3. washthe filter cake was washed with hot methanol (200 mL)
  4. concentrationThe filtrate was concentrated to an approximate volume of 100 mL
  5. extractionextracted with ethyl acetate (400 mL)
  6. washThe organic layer was washed with water and saturated sodium chloride solution
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered through celite®
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2955424da3414e62aa7c1fc187a0884f
출처 데이터셋
uspto-grants-2008_05
특허 번호
US07378414B2

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