تفاعل #10273

معادلة التفاعل

4-benzyl-piperazine-1-carboxylic acid tert-butyl ester

tetramethylethylenediamine

2-(bromomethyl)naphthalene

sec-butyllithium

→

4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester

المذيبات

diethylether

diethylether

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONafter complete addition the solution
2. 2
   درجة الحرارةwas slowly warmed to −10° C., at which temperature the mixture
3. 3
   أخرىwas recooled to −70° C.
4. 4
   workup.STIRRINGstirring
5. 5
   أخرىcontinued at −70° C.
6. 6
   workup.WAITwas continued for one hour
7. 7
   workup.STIRRINGThe resulting mixture was stirred
8. 8
   workup.WAITto come to room temperature overnight
9. 9
   أخرىpartitioned between saturated ammonium chloride (aq) and ethyl acetate
10. 10
    تجفيفThe organic layer was dried over magnesium sulphate
11. 11
    ترشيحfiltered
12. 12
    تركيزconcentrated in vacuo
13. 13
    أخرىThe residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH 99/1)

الإجراء التجريبي

To a solution of 4-benzyl-piperazine-1-carboxylic acid tert-butyl ester (2 g) in diethylether (35 mL) was added tetramethylethylenediamine (1.4 mL). The resulting mixture was cooled to −70° C. and sec-butyllithium (7 mL of a 1.3 M solution) was added dropwise, after complete addition the solution was slowly warmed to −10° C., at which temperature the mixture was stirred for one hour. Subsequently, the mixture was recooled to −70° C.; then a solution of 2-(bromomethyl)naphthalene (2 g) in diethylether was added dropwise and stirring continued at −70° C. was continued for one hour. The resulting mixture was stirred and allowed to come to room temperature overnight, then partitioned between saturated ammonium chloride (aq) and ethyl acetate. The organic layer was dried over magnesium sulphate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH 99/1) to afford 4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester as an oil. 0.8 g (27 %) Rf 0.47 (CH2Cl2/MeOH 99/1), MH+ 417.

المصدر