تفاعل #6074

ord-b9a26e58d0284adca803900d4bbf0d32

معادلة التفاعل

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

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated at 90°-100° C. for 2 hours
  2. 2
    ترشيحthe precipitated solids filtered off
  3. 3
    غسيلwashed with water, and vacuum
  4. 4
    أخرىdried
  5. 5
    أخرىPurification
  6. 6
    أخرىEvaporation of the eluants

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05246955uspto-grants-1993_09