Trifluoroacetic anhydride → N-(3-(1Admantyl)-4-isopropoxyphenethyl)-2,2,2-trifluoro-acetamide

HRID 710451Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 710451
[C:1]12([C:11]3[CH:12]=[C:13]([CH2:21][CH2:22][NH2:23])[CH:14]=[CH:15][C:16]=3[O:17][CH:18]([CH3:20])[CH3:19])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[O:24](C(C(F)(F)F)=O)[C:25]([C:27]([F:30])([F:29])[F:28])=O>>[C:1]12([C:11]3[CH:12]=[C:13]([CH:14]=[CH:15][C:16]=3[O:17][CH:18]([CH3:19])[CH3:20])[CH2:21][CH2:22][NH:23][C:25](=[O:24])[C:27]([F:30])([F:29])[F:28])[CH2:2][CH:3]3[CH2:9][CH:7]([CH2:6][CH:5]([CH2:4]3)[CH2:10]1)[CH2:8]2

Komponenten

3

Edukt 2

HCID 9845Trifluoroacetic anhydrideHCID 667263922-(3-(1-Admantyl)-4-isopropoxyphenyl)ethanamine

Produkt 1

HCID 87126503N-(3-(1Admantyl)-4-isopropoxyphenethyl)-2,2,2-trifluoro-acetamideAusbeute 82,4 %

Versuchsvorschrift

To a stirred solution of 2-(3-(1-Admantyl)-4-isopropoxyphenyl)ethanamine (0.28 g, 0.86 mmol) in a mixture of solvents (CH2Cl2:Et3N: 10:0.5 ml) (CF3CO)2O (0.157 ml) was added at 0° C. under N2. The reaction mixture was stirred for 2 h at room temperature, then the solvent was evaporated to dryness. The residue was diluted to 50 ml with EtOAc and washed with 1M HCl. The organic layer was separated, dried over MgSO4 and filtered. The filtrate was evaporated to dryness to give the title product (0.29 g, 82.4%). 1H-NMR (CDCl3) 1.37 (d, 6H, J=6 Hz); 1.67-1.75 (m, 6H); 2.04-2.23 (m, 9H); 2.78 (tr, 2H, J=6.84 Hz); 3.53-3.59 (m, 2H); 4.57-4.63 (m, 1H); 6.77 (d, 1H, J=8.32 Hz); 6.92 (dd, 1H, J=2.21, 8.27 Hz); 6.98 (d, 1H, J=2.21 Hz).

Aufarbeitung

  1. additionwas added at 0° C. under N2
  2. customthe solvent was evaporated to dryness
  3. additionThe residue was diluted to 50 ml with EtOAc
  4. washwashed with 1M HCl
  5. customThe organic layer was separated
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customThe filtrate was evaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-0eb14a34d4b94b729ae8c5e67395e459
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09181182B2

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