تفاعل #2075727

ord-09fc7af3ff7341b9b21214560c44e4d2

معادلة التفاعل

C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
lithium bis(trimethylsilyl)amide
COc1c(Cl)ccc(C#N)c1F
4-chloro-2-fluoro-3-methoxybenzonitrile
CC(C)O
2-propanol
Cl
HCl
COc1c(Cl)ccc(C(=N)N)c1F.Cl
title compound
المردود 156.9%
COc1c(Cl)ccc(C(=N)N)c1F.Cl
4-Chloro-2-fluoro-3-methoxybenzamidine hydrochloride
المردود 156.9%

المذيبات

ظروف التفاعل

درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITUpon standing at 5° C. for 18 h
  2. 2
    أخرىprecipitated
  3. 3
    ترشيحThe precipitated product was collected by filtration
  4. 4
    غسيلwashed with ether
  5. 5
    أخرىdried under vacuum

الإجراء التجريبي

4-chloro-2-fluoro-3-methoxybenzonitrile (3.0 g, 16 mmol) was dissolved in 7 mL dry THF and added dropwise to a 1M solution of lithium bis(trimethylsilyl)amide (18 mL, 18 mmol). After stirring at 25° C. for 5 h, the mixture was treated with 25 mL of 2-propanol saturated with gaseous HCl. Upon standing at 5° C. for 18 h, the mixture was diluted with 30 mL ether whereupon the product precipitated. The precipitated product was collected by filtration, washed with ether and dried under vacuum to give the title compound (3.0 g, 78.6% yield): 1H NMR (DMSO-d6) δ 9.70 (br d, 3H), 7.58 (m, 1H), 7.46 (m, 1H), 7.39 (br d, 1H), 3.96 (s, 3H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07642220B2uspto-grants-2010_01