تفاعل #2286337

ord-114f2847e7e94f64ab9711790325f10a

معادلة التفاعل

O=[N+]([O-])c1cc(Cl)c(O)c(Cl)c1
2,6-dichloro-4-nitro-phenol
C1CN2CCN1CC2
1,4-diazabicyclo[2.2.2]octane
CN(C)C(=S)Cl
dimethylthiocarbamoyl chloride
CN(C)C(=S)Oc1c(Cl)cc([N+](=O)[O-])cc1Cl
dimethyl-thiocarbamic acid O-(2,6-dichloro-4-nitro-phenyl)ester
المردود 75.3%
CN(C)C(=S)Oc1c(Cl)cc([N+](=O)[O-])cc1Cl
Dimethyl-thiocarbamic acid O-(2,6-dichloro-4-nitro-phenyl)ester
المردود 75.3%

ظروف التفاعل

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

المعالجة

  1. 1
    غسيلwas then washed with a 1N aqueous hydrochloric acid solution (1×125 mL), water (1×125 mL)
  2. 2
    تجفيفa saturated aqueous sodium chloride solution (1×125 mL), dried with magnesium sulfate
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated under vacuum

الإجراء التجريبي

A solution of 2,6-dichloro-4-nitro-phenol (3.0 g, 14.4 mmol) in N,N-dimethylformamide (70 mL) at 25° C. was treated with 1,4-diazabicyclo[2.2.2]octane (3.16 mL, 28.8 mmol) and dimethylthiocarbamoyl chloride (2.85 g, 23.04 mmol). The reaction was stirred at 25° C. for 18 h. At this time, the reaction was diluted with ethyl acetate (250 mL) and was then washed with a 1N aqueous hydrochloric acid solution (1×125 mL), water (1×125 mL), and a saturated aqueous sodium chloride solution (1×125 mL), dried with magnesium sulfate, filtered and concentrated under vacuum. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 80:20 petroleum ether/ethyl acetate) afforded dimethyl-thiocarbamic acid O-(2,6-dichloro-4-nitro-phenyl)ester (79) (3.2 g, 75%) as a white solid; EL-LRMS for C9H8Cl2N2O3S (M−Cl)+ at m/z=259. Exact Mass=293.9633; Molecular weight=295.15

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE046024E1uspto-grants-2016_06