تفاعل #735521

معادلة التفاعل

N-t-butoxycarbonyl-D-alanine

hydrochloric acid

ethyl chloroformate

2-methylthio-2,4-dimethyl-3-aminopentane

triethylamine

→

D-Alanine N-(2-methylthio-2,4-dimethylpentan-3-yl)amide

المذيبات

tetrahydrofuran

ethyl acetate

methanol

butanol water acetic acid

ظروف التفاعل

المعالجة

1. 1
   workup.STIRRINGthe mixture stirred for one hour
2. 2
   غسيلwashed with water, 5% aqueous citric acid (w/v), sodium bicarbonate solution and brine
3. 3
   أخرىThe organic phase was evaporated
4. 4
   أخرىto provide 6.0 g
5. 5
   درجة الحرارةthe mixture refluxed for one hour
6. 6
   أخرىAfter evaporation of methanol
7. 7
   غسيلwashed with ether
8. 8
   استخلاصextracted wtih ethyl ether
9. 9
   أخرىEvaporation of the extracts
10. 10
    أخرىgave 3.2 g

الإجراء التجريبي

To a solution of 3.2 g. (0.017 mole) N-t-butoxycarbonyl-D-alanine and 2.5 g. (0.017 mole) triethylamine in 100 ml. of tetrahydrofuran at -15° C. was added 1.63 ml. of ethyl chloroformate. After stirring for 15 minutes, 2.49 g. (0.017 mole) 2-methylthio-2,4-dimethyl-3-aminopentane was added and the mixture stirred for one hour. The reaction mixture was diluted with ethyl acetate, washed with water, 5% aqueous citric acid (w/v), sodium bicarbonate solution and brine. The organic phase was evaporated to provide 6.0 g. of residue. This was taken up in 100 ml. methanol, 60 ml. of concentrated hydrochloric acid added and the mixture refluxed for one hour. After evaporation of methanol, the residue was taken up in water, washed with ether, the aqueous phase adjusted to pH 12 with sodium hydroxide and extracted wtih ethyl ether. Evaporation of the extracts gave 3.2 g. (87%) of product as a colorless oil Rf 0.56 (butanol/water/acetic acid-4:1:1 by volume).

المصدر