تفاعل #487553
ord-02c91f9ad526464ca82270c8c7cf6b98
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1workup.DISSOLUTIONdissolves
- 2درجة الحرارةmaintaining the temperature at 0-5° C
- 3workup.ADDITIONOnce the addition
- 4أخرىthe cooling bath is removed
- 5workup.STIRRINGthe reaction mixture is stirred for one hour at room temperature
- 6workup.STIRRINGThe reaction mixture is stirred
- 7درجة الحرارةto warm to room temperature over three hours
- 8استخلاصThe mixture is extracted with diethyl ether
- 9تجفيفdried over anhydrous sodium sulfate
- 10ترشيحfiltered
- 11تركيزthe filtrate is concentrated in vacuo
- 12أخرىThe residue is further purified by column chromatography on silica gel
- 13غسيلeluting with hexane
الإجراء التجريبي
Hydrobromic acid (48% wt. in water, 240 ml) is added dropwise to a suspension of 4-ethyl-3-nitroaniline (20 g, 0.12 mol) in water (80 ml), and the mixture is stirred until the solid dissolves. The mixture is cooled to −5° C. and a solution of sodium nitrite (19.8 g, 0.28 mol) in water (100 ml) is added dropwise, maintaining the temperature at 0-5° C. Once the addition is complete, the cooling bath is removed and the reaction mixture is stirred for one hour at room temperature. The mixture is added dropwise to a pre-cooled solution of cuprous bromide (22.4 g, 0.16 mol) in hydrobromic acid (48% wt. in water) at 0° C. The reaction mixture is stirred and allowed to warm to room temperature over three hours. The mixture is extracted with diethyl ether, and the organic extracts are combined, dried over anhydrous sodium sulfate, filtered and the filtrate is concentrated in vacuo. The residue is further purified by column chromatography on silica gel, eluting with hexane to give 4-bromo-1-ethyl-2-nitrobenzene (18 g)