تفاعل #56461

ord-b39752b53b1947aa81e876ffdc1c2b70

معادلة التفاعل

O=C(O)CCl
chloroacetic acid
[Na+].[OH-]
sodium hydroxide
OCc1ccc2c(c1)OCO2
piperonyl alcohol
NC(=[NH2+])S
thiouronium
Cl
HCl
NC(N)=S
thiourea
Br
hydrobromic acid
CC(C)OC(C)C
diisopropyl ether
O=C([O-])O
bicarbonate
OC(=S)CCc1ccc2c(c1)OCO2
said acid
المردود 52.8%
OC(=S)CCc1ccc2c(c1)OCO2
3,4-Methylenedioxybenzylthio-acetic acid
المردود 52.8%

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىequipped with a magnetic stirrer and a condenser
  2. 2
    درجة الحرارةThe temperature is raised to 95° C.
  3. 3
    درجة الحرارةto cool
  4. 4
    ترشيحthese are filtered off
  5. 5
    أخرىThe precipitate thus obtained
  6. 6
    درجة الحرارةThe mixture is heated to 70° C.
  7. 7
    درجة الحرارةThe whole is then heated
  8. 8
    درجة الحرارةunder reflux for half an hour
  9. 9
    درجة الحرارةafter which it is cooled
  10. 10
    أخرىthe precipitate obtained
  11. 11
    workup.DISSOLUTIONis redissolved in
  12. 12
    غسيلthe solution is washed with methylene chloride
  13. 13
    ترشيحfiltered over charcoal
  14. 14
    أخرىto precipitate 3,4-methylenedioxybenzylthio-acetic acid, which
  15. 15
    ترشيحis filtered off
  16. 16
    أخرىAfter recrystallisation

الإجراء التجريبي

A solution of 18.24 g (0.24 mol) of thiourea in 104 ml of 48% strength hydrobromic acid and 20 ml of water is introduced into a one liter three-necked flask equipped with a magnetic stirrer and a condenser. The mixture is heated to 60° C. and 30.4 g (0.2 mol) of piperonyl alcohol are introduced. The temperature is raised to 95° C. and the mixture is allowed to cool. Crystals of thiouronium salt appear; these are filtered off and suction-drained. The precipitate thus obtained is introduced into a 500 ml three-necked flask together with 60 ml of sodium hydroxide solution. The mixture is heated to 70° C. and 15.6 g (0.164 mol) of chloroacetic acid in 30 ml of water are added dropwise. The whole is then heated under reflux for half an hour, after which it is cooled. The mixture is acidified with 3N HCl, the precipitate obtained is redissolved in a dilute (sodium) bicarbonate solution, and the solution is washed with methylene chloride, filtered over charcoal and again acidified with 3N HCl so as to precipitate 3,4-methylenedioxybenzylthio-acetic acid, which is filtered off. After recrystallisation from a 1:1 (volume/volume) mixture of diisopropyl ether and petroleum ether, 18.2 g (40% yield) of the said acid (instantaneous melting point=87° C.) are collected.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04225617uspto-grants-1980_09