Toluene → 2,2,4,6,7-Pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amine

HRID 2253354노트

반응식

HRID 2253354 반응식
C([NH:8][C:9]1[C:10]([CH3:29])=[C:11]([CH3:28])[C:12]2[O:16][C:15]([CH3:18])([CH3:17])[CH:14]([C:19]3[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=3)[C:13]=2[C:26]=1[CH3:27])C1C=CC=CC=1.C1(C)C=CC=CC=1.C(O)(C)C>[Pd].[C].O>[CH3:17][C:15]1([CH3:18])[CH:14]([C:19]2[CH:20]=[CH:21][C:22]([CH3:25])=[CH:23][CH:24]=2)[C:13]2[C:26]([CH3:27])=[C:9]([NH2:8])[C:10]([CH3:29])=[C:11]([CH3:28])[C:12]=2[O:16]1

참가 물질

6

반응 조건

온도
50 °C

실험 절차

To a mixture of N-benzyl-2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amine (80 g), toluene (240 mL) and isopropanol (80 mL) was added 10% Pd-carbon (a product containing 50% water, 4 g), and the mixture was hydrogenated at 35° C. under atmospheric pressure. After completion of the reaction, the catalyst was filtered. Concentrated hydrochloric acid (19.2 mL) was added to the filtrate and the mixture was stirred at 10° C. or below for 1 hour. Precipitated crystals were filtered. The crystals were added to a mixture of methanol (560 mL) and water (80 mL) and the mixture was heated to 50° C. to dissolve the crystals. Then, 25% aqueous ammonia water was added dropwise to the solution to adjust to pH 8.5. Precipitated crystals were filtered to obtain the title compound (54.32 g, 88.6%).

후처리

  1. customwas hydrogenated at 35° C. under atmospheric pressure
  2. customAfter completion of the reaction
  3. filtrationthe catalyst was filtered
  4. additionConcentrated hydrochloric acid (19.2 mL) was added to the filtrate
  5. customPrecipitated crystals
  6. filtrationwere filtered
  7. additionThe crystals were added to a mixture of methanol (560 mL) and water (80 mL)
  8. dissolutionto dissolve the crystals
  9. additionThen, 25% aqueous ammonia water was added dropwise to the solution
  10. customPrecipitated crystals
  11. filtrationwere filtered

출처 및 근거

ORD 기록
ord-316d46839f3e42caa377f8c8406edb69
출처 데이터셋
uspto-grants-2008_01
특허 번호
US07323577B2

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