تفاعل #1265372

ord-ccdc4f37c33149caa8e89f13fb5d03f4

معادلة التفاعل

O=C(Cl)OCC(Cl)(Cl)Cl
2,2,2-trichloroethyl chloroformate
Cc1ccc(-n2nc(C(C)(C)C)cc2N)cc1.Cl
5-amino-3-t-butyl-1-p-tolylpyrazole hydrochloride
O
water
[Na+].[OH-]
NaOH
Cc1ccc(-n2nc(C(C)(C)C)cc2NC(=O)OCC(Cl)(Cl)Cl)cc1
5-(2,2,2-Trichloroethoxycarbonyl)amino-3-t-butyl-1-p-tolylpyrazole

المذيبات

ظروف التفاعل

درجة الحرارة
10°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was stirred at room temperature for 2 h
  2. 2
    أخرىthe aqueous layer was separated from the EtOAc layer
  3. 3
    غسيلThe EtOAc layer was washed with brine (2×0.9 L)
  4. 4
    تجفيفdried over MgSO4 (60 g)
  5. 5
    ترشيحThe EtOAc layer was collected by filtration
  6. 6
    workup.ADDITIONTo this solution, heptane was added
  7. 7
    أخرىA part of the solution was removed by distillation
  8. 8
    أخرىThe product was crystallized from the solution
  9. 9
    ترشيحcollected by filtration
  10. 10
    أخرىdried in vacuum oven to constant weight

الإجراء التجريبي

A mixture of 5-amino-3-t-butyl-1-p-tolylpyrazole hydrochloride (300 g, 1.13 mol), water (0.9 L), EtOAc (2.1 L) and NaOH (117 g, 2.84 mol) was stirred between 5-15° C. for 30 min. To this mixture, 2,2,2-trichloroethyl chloroformate (342 g, 1.58 mol) was added over 1 h between 5-15° C. The mixture was stirred at room temperature for 2 h, and then the aqueous layer was separated from the EtOAc layer. The EtOAc layer was washed with brine (2×0.9 L) and dried over MgSO4 (60 g). The EtOAc layer was collected by filtration. To this solution, heptane was added. A part of the solution was removed by distillation. The product was crystallized from the solution, collected by filtration and dried in vacuum oven to constant weight. Yield: 409 g, 90%. 1H NMR (CDCl3) 7.40 (d, 2H), 7.30 (d, 2H), 6.40 (s, 1H), 4.80 (s, 2H), 2.40 (s, 3H), 1.40 (s, 9H). MS (EI) m/z 404 (M+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07276491B2uspto-grants-2007_10