تفاعل #49766

ord-e6b45e217a2842468d658089a3c18c68

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter completion of the reaction
  2. 2
    أخرىthe catalyst was separated by filtration
  3. 3
    تجفيفthe resulting filtrate was dried with anhydrous magnesium sulfate
  4. 4
    أخرىAfter separating the drying agent
  5. 5
    ترشيحby filtration
  6. 6
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure from the filtrate

الإجراء التجريبي

Benzyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate (2.00 g, 5.51 mmol) synthesized as described above, 5% Pd/C (100 mg) as a catalyst, and toluene (15 ml) as a solvent were charged into a 50 cc round-bottom flask, and the inside of the flask was replaced sufficiently with a hydrogen gas. Then, in a hydrogen gas atmosphere, the mixture was thoroughly stirred for 3 hours at 50° C. After completion of the reaction, the catalyst was separated by filtration, the resulting filtrate was dried with anhydrous magnesium sulfate. After separating the drying agent by filtration, the solvent was distilled off under reduced pressure from the filtrate to obtain quantitatively 2-fluoro-4-chloro-5-cyclopentyloxyaniline (1.26 g) as a pale brown oily substance. The spectral data and the like are shown in Reference Example 1.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05424277uspto-grants-1995_06