تفاعل #60448

معادلة التفاعل

2-(3,3,4,4-tetramethylcyclopent-1-enyl)phenylamine

bis(2-chloroethyl)amine hydrochloride

→

title compound

المردود 50.9%

1-[2-(3,3,4,4-Tetramethylcyclopent-1-enyl)phenyl]piperazine

المردود 50.9%

المذيبات

1,2-dichlorobenzene

ظروف التفاعل

المعالجة

1. 1
   أخرىDuring the reaction
2. 2
   أخرىto remove the hydrogen chloride gas in the reactor
3. 3
   درجة الحرارةThe reaction mixture was air-cooled to room temperature
4. 4
   workup.ADDITIONaqueous solution of potassium carbonate, ethyl acetate and methanol were added
5. 5
   استخلاصextraction
6. 6
   تجفيفThe obtained organic layers were dried over anhydrous sodium sulfate
7. 7
   ترشيحThe desiccant was filtered off
8. 8
   تركيزthe filtrate was concentrated under reduced pressure
9. 9
   أخرىThe obtained residue was purified by NH silica gel column chromatography (ethyl acetate/heptane)

الإجراء التجريبي

A mixture of 2-(3,3,4,4-tetramethylcyclopent-1-enyl)phenylamine (331 mg, 1.54 mmol) produced in Example (54c), 1,2-dichlorobenzene (4.7 mL) and bis(2-chloroethyl)amine hydrochloride (330 mg, 1.85 mmol) was stirred for 9 hours at an external temperature of 200° C. under a nitrogen atmosphere. During the reaction, a nitrogen stream was blown into the reactor several times to remove the hydrogen chloride gas in the reactor. The reaction mixture was air-cooled to room temperature, and then aqueous solution of potassium carbonate, ethyl acetate and methanol were added and extraction was performed three times with ethyl acetate. The obtained organic layers were dried over anhydrous sodium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The obtained residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 223 mg of the title compound as a brown oil.

المصدر