تفاعل #362621

ord-912ed703e1954c0a984471dd243a718c

معادلة التفاعل

Oc1cccc(F)c1
m-fluorophenol
COC(=O)C(C)Cl
methyl 2-chloropropionate
Cl
HCl
CC(Oc1cccc(F)c1)C(=O)O
2-(3' -fluorophenoxy)propionic acid
المردود 42.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto cool
  2. 2
    أخرىreached about 40° C.
  3. 3
    درجة الحرارةto cool to room temperature
  4. 4
    استخلاصThe reaction mixture was extracted twice with 100 ml ethyl ether
  5. 5
    غسيلwashed with 200 ml of 1.5M aqueous sodium carbonate
  6. 6
    أخرىThe aqueous layer was separated
  7. 7
    workup.ADDITIONby adding concentrated HCl
  8. 8
    استخلاصThe acidified aqueous layer was extracted with 200 ml ethyl ether
  9. 9
    أخرىThe organic layer was separated
  10. 10
    تجفيفdried with MgSO4
  11. 11
    ترشيحfiltered
  12. 12
    أخرىThe solvent was removed in vacuo

الإجراء التجريبي

To a solution of m-fluorophenol (24.2 g, 0.22 mol) in 79.2 ml of 25% aqueous sodium hydroxide heated to 45° C. with an oil bath was added 29.5 ml (0.26 mol) methyl 2-chloropropionate. The reaction mixture was heated to 80° C. for 17 hours and then allowed to cool. When the temperature reached about 40° C., concentrated HCl (25 ml) was added and the reaction mixture was allowed to cool to room temperature. The reaction mixture was extracted twice with 100 ml ethyl ether. The organic layers were combined and washed with 200 ml of 1.5M aqueous sodium carbonate. The aqueous layer was separated and acidified to pH 1, by pH test paper, by adding concentrated HCl. The acidified aqueous layer was extracted with 200 ml ethyl ether. The organic layer was separated, dried with MgSO4 and filtered. The solvent was removed in vacuo to yield 17 g (41% yield) of 2-(3' -fluorophenoxy)propionic acid as a yellow solid (m.p. 72.5°-74° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05393735uspto-grants-1995_02