반응 #710557

ord-716a6551883c4bf493a4b1613ee788e9

반응 방정식

Cl
HCl
CN(C)C(=O)c1ccc(OC/C(=C\F)CNC(=O)OC(C)(C)C)cc1
(Z)-tert-butyl 2-((4-(dimethylcarbarnoyl)-phenoxy)methyl)-3-fluoroallylcarbamate
O=C(O)C(F)(F)F
trifluoroacetic acid
CN(C)C(=O)c1ccc(OC/C(=C\F)CN)cc1.Cl
(Z)-4-(2-(aminomethyl)-3-fluoroallyloxy)-N,N-dimethylbenzamide hydrochloride
수율 71.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타All volatiles were removed in vacuo
  2. 2
    기타to remove trifluoroacetic acid
  3. 3
    기타The precipitate formed
  4. 4
    기타was isolated
  5. 5
    기타dried under reduced pressure

실험 절차

To a stirring solution of (Z)-tert-butyl 2-((4-(dimethylcarbarnoyl)-phenoxy)methyl)-3-fluoroallylcarbamate (520.0 mg, 1.48 mmol) in CH2Cl2 (8.0 mL) at room temperature was added trifluoroacetic acid (2.0 mL). The resulting mixture was stirred at room temperature for 30 min. All volatiles were removed in vacuo and the residue was co-evaporated with CH2Cl2 (2×20 mL) to remove trifluoroacetic acid. The resulting oil was taken up in ethyl acetate (3.0 mL) and then ethereal HCl (2.0 M in diethyl ether; 1.0 mL, 2.0 mmol) was added. The precipitate formed was isolated and dried under reduced pressure to afford (Z)-4-(2-(aminomethyl)-3-fluoroallyloxy)-N,N-dimethylbenzamide hydrochloride (301 mg, 71%) as a pale yellow solid; m.p.=135-137° C.; 1H-NMR (300 MHz; MeOD) δ ppm: 3.06 (3H, br s), 3.10 (3H, br s), 3.71 (2H, d, J 3.0 Hz), 4.88 (2H, dd, J 2.8, 0.8 Hz), 7.11 (2H, d, J 8.9 Hz), 7.13 (1H, d, J 80.8 Hz), 7.45 (2H, d, J 8.9 Hz).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09302986B2uspto-grants-2016_04