1-[4-(Benzyloxy)-2-hydroxy-3-nitrophenyl]ethan-1-one → 1-(3-Amino-4-(benzyloxy)-2-hydroxyphenyl)ethanone

HRID 1689215노트

반응식

HRID 1689215 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15](=[O:17])[CH3:16])=[C:11]([OH:18])[C:10]=1[N+:19]([O-])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)(=O)C.[Zn]>[NH2:19][C:10]1[C:11]([OH:18])=[C:12]([C:15](=[O:17])[CH3:16])[CH:13]=[CH:14][C:9]=1[O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

4

반응물 1

HCID 579889911-[4-(Benzyloxy)-2-hydroxy-3-nitrophenyl]ethan-1-one

생성물 1

HCID 579892521-(3-Amino-4-(benzyloxy)-2-hydroxyphenyl)ethanone

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

Zinc dust (5.5 g) was added portionwise to a suspension of 1-(4-(benzyloxy)-2-hydroxy-3-nitrophenyl)ethanone (example 11, step b) (5.5 g) in acetic acid (55 mL) over 15 minutes, whilst maintaining the internal temperature below 40° C. with an ice bath. The mixture was allowed to attain ambient temperature and stirred for 2 h. The mixture was filtered through Celite (Caution: Gets hot—do not allow to dry), washed with acetic acid, and the filtrate poured onto ice/water (500 mL). The resulting precipitate was filtered off, washed with water, and dried under vacuum at 40° C. to afford the subtitled compound as a light brown solid. Yield 4.8 g.

후처리

  1. temperaturewhilst maintaining the internal temperature below 40° C. with an ice bath
  2. customto attain ambient temperature
  3. filtrationThe mixture was filtered through Celite (Caution
  4. customto dry),
  5. washwashed with acetic acid
  6. additionthe filtrate poured onto ice/water (500 mL)
  7. filtrationThe resulting precipitate was filtered off
  8. washwashed with water
  9. customdried under vacuum at 40° C.

출처 및 근거

ORD 기록
ord-da37aae32a44434697388ff6f4081380
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08148373B2

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