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Methylamine → 1-(3-Methoxyphenyl)-N-methylethanamine

HRID 1666313
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HRID 1666313 반응식
[CH3:1][NH2:2].[CH3:3][O:4][C:5]1[CH:6]=[C:7]([CH:16]=[CH:17][CH:18]=1)[C:8]([C:10]1C=CC=CC=1)=O.[BH4-].[Na+]>CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].O>[CH3:3][O:4][C:5]1[CH:6]=[C:7]([CH:8]([NH:2][CH3:1])[CH3:10])[CH:16]=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6329MethylamineHCID 4311764Sodium borohydrideHCID 12451863(3-Methoxyphenyl)(phenyl)methanone

생성물 1

HCID 148716881-(3-Methoxyphenyl)-N-methylethanamine

시약·촉매·용매 2

HCID 11026Titanium isopropoxide촉매HCID 962Water용매

실험 절차

Titanium(IV) isopropoxide (130 ml) was added to a methanolic methylamine solution (125 ml, 8M) followed by the addition of 3-methoxybenzophenone (50 g). The reaction mixture was stirred at room temperature for 5 hours, after which sodium borohydride (12 g) was carefully added at 0-5° C. The mixture was stirred at room temperature for 2 hours, after which water (60 ml) was added. The inorganic precipitate was filtered off and the filtrate concentrated to dryness. The residue was partitioned between ethyl acetate (400 ml) and aqueous hydrochloric acid (2M, 400 ml). The aqueous phase was made alkaline (pH 11-12) and extracted with dichloromethane (2×300 ml). The organic phase was dried and concentrated to dryness, leaving 1-(3-methoxyphenyl)-N-methylethylamine (43.4 g) as a viscous oil.

후처리

  1. stirringThe mixture was stirred at room temperature for 2 hours
  2. filtrationThe inorganic precipitate was filtered off
  3. concentrationthe filtrate concentrated to dryness
  4. customThe residue was partitioned between ethyl acetate (400 ml) and aqueous hydrochloric acid (2M, 400 ml)
  5. extractionextracted with dichloromethane (2×300 ml)
  6. customThe organic phase was dried
  7. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-d91dfa7fb3724a34919901491a62c8b0
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044067B2

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