تفاعل #63942

ord-9d69bf3a04044b388d423dcf70b25191

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAcidification with 6.0N hydrochloric acid precipitated the crude naphthalene ester product
  2. 2
    ترشيحThe solid was filtered
  3. 3
    غسيلwashed with water
  4. 4
    أخرىrecrystallized from aqueous methanol

الإجراء التجريبي

A solution of 10.2 g (0.033 mole) of 1,2,3,4-tetrahydro-2-bromo-6-methoxy-1-oxo-2-naphthalenecarboxylic acid, methyl ester in 100 ml of tetrahydrofuran under a nitrogen atmosphere was treated over 15 minutes with a solution of 10.0 ml (10.2 g; 0.067 mole) of 1,8-diazabicyclo[5.4.0]undec-7-ene in 20 ml of tetrahydrofuran. The mixture was stirred at room temperature for 16 hours, then added to 450 g of ice/water. Acidification with 6.0N hydrochloric acid precipitated the crude naphthalene ester product. The solid was filtered, washed with water, and recrystallized from aqueous methanol to yield 5.1 g (67% yield) of the final product, mp 109°-111°. This material was identical with that prepared by the procedure described in Example 11.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04767776uspto-grants-1988_08