تفاعل #1509575

ord-62cbb12001e04407a5020d1349c3fac1

معادلة التفاعل

Cn1nnnc1-c1cc(Br)cc([N+](=O)[O-])c1
5-(3-Bromo-5-nitro-phenyl)-1-methyl-1H-tetrazole
Cn1nnnc1-c1cc(N)cc(Br)c1
title compound
المردود 15.4%
Cn1nnnc1-c1cc(N)cc(Br)c1
3-Bromo-5-(1-methyl-1H-tetrazol-5-yl)-phenylamine
المردود 15.4%

الكواشف

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas hydrogenated on a H-cube® apparatus at 20° C.
  2. 2
    أخرىAfter reaction completion
  3. 3
    تركيزthe mixture was concentrated in vacuum
  4. 4
    أخرىtriturated with MeOH
  5. 5
    ترشيحThe solid was filtered
  6. 6
    أخرىfurther triturated
  7. 7
    أخرىair-dried

الإجراء التجريبي

A solution of 5-(3-Bromo-5-nitro-phenyl)-1-methyl-1H-tetrazole (2.1 g) in EtOAc (100 ml) was hydrogenated on a H-cube® apparatus at 20° C., room pressure with a flow rate of 1 ml/min using a Raney-Ni cartridge. After reaction completion, the mixture was concentrated in vacuum and triturated with MeOH. The solid was filtered and further triturated and air-dried to give the title compound (290 mg). Rt 1.25 min (method D).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE045323E1uspto-grants-2015_01