تفاعل #335359

ord-aaa6707d54f14cdf803fde042812c2cf

معادلة التفاعل

ClCc1ccc2ccccc2n1
2-(Chloromethyl)quinoline
CC(C(=O)O)c1ccc2cc(O)ccc2c1
6-hydroxy-α-methyl-2-naphthaleneacetic acid
C[O-].[Na+]
sodium methoxide
CC(C(=O)O)c1ccc2cc(OCc3ccc4ccccc4n3)ccc2c1
oil
المردود 151.1%
CC(C(=O)O)c1ccc2cc(OCc3ccc4ccccc4n3)ccc2c1
α-Methyl-6-(2-quinolinylmethoxy)-2-naphthaleneacetic acid
المردود 151.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter 10 minutes the solvent is removed
  2. 2
    أخرىThe reaction mixture is partitioned between water and methylene chloride
  3. 3
    غسيلthe organic layer is washed with water
  4. 4
    أخرىevaporated

الإجراء التجريبي

To a solution of 6-hydroxy-α-methyl-2-naphthaleneacetic acid (10.8 g, 50 mmol) in methanol (100 ml) is added sodium methoxide (100 mmol). After 10 minutes the solvent is removed and replaced with dimethylformamide (250 ml). 2-(Chloromethyl)quinoline (17.8 g, 100 mmol) is then added and the reaction mixture is stirred for 8 days at room temperature. The reaction mixture is partitioned between water and methylene chloride, the organic layer is washed with water and evaporated to yield 27 g of an oil. Recrystallization of this oil twice from acetonitrile gives 10.6 g of white crystals of intermediate ether ester (42% yield, m.p. 106°-108° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05208344uspto-grants-1993_05