تفاعل #9724

ord-cde935c22f454ba4aabd0f9182db7aa1

معادلة التفاعل

Cl
hydrochloric acid
CCOC(=O)C(C)(C)Oc1ccc(OC(C)=O)cc1C
ethyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoate
CCOC(=O)C(C)(C)Oc1ccc(OC(C)=O)cc1C
intermediate 9
CCOC(=O)C(C)(C)Oc1ccc(OC(C)=O)cc1C
ethyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoate
CC[O-].[Na+]
sodium ethoxide
CCOC(=O)C(C)(C)Oc1ccc(O)cc1C
title compound
CCOC(=O)C(C)(C)Oc1ccc(O)cc1C
ethyl 2-(4-hydroxy-2-methylphenoxy)-2-methylpropanoate

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزthe solution concentrated
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in t-butylmethyl ether
  3. 3
    غسيلthe resulting solution washed with water
  4. 4
    تجفيفdried over sodium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    تركيزthe filtrate concentrated
  7. 7
    أخرىto give a brown oil
  8. 8
    أخرىFurther purification by Biotage® chromatography
  9. 9
    غسيلeluting initially with cyclohexane

الإجراء التجريبي

A solution of ethyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoate (intermediate 9, 40.8 g) in ethanol (280 ml) was treated with sodium ethoxide (12.9 g) at room temperature under nitrogen. The resulting solution was heated to 50° C. for 1 hour. 2M hydrochloric acid (95 ml) was added to the cooled reaction and the solution concentrated. The residue was dissolved in t-butylmethyl ether and the resulting solution washed with water followed by brine and then dried over sodium sulfate, filtered and the filtrate concentrated to give a brown oil. Further purification by Biotage® chromatography eluting initially with cyclohexane and then cyclohexane:ethyl acetate (5:1) gave the title compound as an orange oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091237B2uspto-grants-2006_08