반응 #6074

ord-b9a26e58d0284adca803900d4bbf0d32

반응 방정식

Cc1cc(Br)c([N+](=O)[O-])cc1[N+](=O)[O-]
5-bromo-2,4-dinitrotoluene
C1CCNC1
pyrrolidine
Cc1cc(N2CCCC2)c([N+](=O)[O-])cc1[N+](=O)[O-]
17
Cc1cc(N2CCCC2)c([N+](=O)[O-])cc1[N+](=O)[O-]
2,4-Dinitro-5-N-pyrrolidinotoluene

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated at 90°-100° C. for 2 hours
  2. 2
    여과the precipitated solids filtered off
  3. 3
    세척washed with water, and vacuum
  4. 4
    기타dried
  5. 5
    기타Purification
  6. 6
    기타Evaporation of the eluants

실험 절차

A mixture of 5-bromo-2,4-dinitrotoluene (2.61 g, 10 mmol) and pyrrolidine (2.49 g, 35 mmol) was heated at 90°-100° C. for 2 hours. The resulting dark brown oil was combined with cracked ice and the precipitated solids filtered off, washed with water, and vacuum dried. Purification was carried out by flash chromatography of the solids on a silica gel column using chloroform/hexane (50:50) as eluant. Evaporation of the eluants afforded 17 as orange needles: 2.0 g (82%) yield; mp 142° C.; TLC (chloroform), Rf =0.82; IR (KBr pellet) 1606, 1566, 1510, 1369, 1350, 1334, 1301, 1276, 1130, 833 cm-1 ; 1H NMR (dimethyl sulfoxide-d6) δ8.83 and 8 53 (2H, 2×s, aromatic protons), 3.27 (4H, m, methylenes adjacent to pyrrolidine N), 2.61 (3H, s, methyl), 1.99 (4H, m, other pyrrolidine methylenes); mass spectrum (EI mode) m/z 251 (P+), 234 (P+ -OH). Anal. Calcd for C11H13N3O4 : C, 52.58; H, 5.21; N, 16.72. Found: C, 52.51; H, 5 27; N, 16.64.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05246955uspto-grants-1993_09