تفاعل #685033

ord-e970d7ef62814bfc9724f96464d27816

معادلة التفاعل

COc1ccc(C=O)cc1
4-methoxybenzaldehyde
CC(C)(C)OC(=O)NN
tert-butyl carbazate
COc1ccc(/C=N/NC(=O)OC(C)(C)C)cc1
title compound
المردود 102.0%
COc1ccc(/C=N/NC(=O)OC(C)(C)C)cc1
(E)-tert-Butyl 2-(4-methoxybenzylidene)hydrazinecarboxylate
المردود 102.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةHeat
  2. 2
    درجة الحرارةto reflux over a period of 1 hour (h)
  3. 3
    أخرىcollecting water in an azeotrope with the toluene
  4. 4
    أخرىAfter no further water is collected
  5. 5
    أخرىAdd hexanes until the product precipitates from solution
  6. 6
    درجة الحرارةCool the bath further to 20° C
  7. 7
    أخرىCollect the solids
  8. 8
    ترشيحby filtration
  9. 9
    أخرىdry

الإجراء التجريبي

Add 4-methoxybenzaldehyde (400 g, 2.94 mol) over 20 min to a solution of tert-butyl carbazate (400 g, 2.94 mol) in toluene (750 mL) at 50° C. Heat to reflux over a period of 1 hour (h), collecting water in an azeotrope with the toluene. After no further water is collected, cool to 60° C. Add hexanes until the product precipitates from solution. Cool the bath further to 20° C. Collect the solids by filtration and dry using a nitrogen press to afford the title compound (750.5 g, 91%). 1H NMR [400 MHz, dimethyl sulfoxide-d6 (DMSO-d6)] δ 10.6-10.8 (bs, 1H), 7.88-8.0 (S, 1H), 7.5-7.55 (d, 2H), 6.95-7.0 (d, 2H), 1.45 (s, 9H). ES/MS (m/z): 249 [M-H].

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897600B2uspto-grants-2011_03