تفاعل #657229

ord-12797a04953149c0aadb673dd30e6536

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared in a similar manner
  2. 2
    استخلاصextracted with diethylether
  3. 3
    استخلاصextracted with diethylether
  4. 4
    غسيلThe organic phase was washed with water
  5. 5
    تجفيفdried over sodium sulphate
  6. 6
    أخرىEvaporation of the solvent under reduced pressure

الإجراء التجريبي

A mixture of the two diastereoisomers of 2-(1-bromoethyl)-2-(6-methoxy-2-naphthyl)-1,3-dioxolane-4(R),5(R)-dicarboxylic acid diethyl ester 3 and 4 (prepared in a similar manner as described in the example 1) (21.18 g, 0.044 mol, ratio 3:4=1:1), sodium hydroxide (3.52 g, 0.088 mol), dimethoxyethane (35 ml) and of water (35 ml) was kept, under stirring, at room temperature for 2 hours. The reaction mixture was diluted with water and extracted with diethylether. The aqueous phase was acidified with concentrated hydrochloric acid to pH 1 and extracted with diethylether. The organic phase was washed with water and dried over sodium sulphate. Evaporation of the solvent under reduced pressure gave the two diastereoisomers of 2-(1-bromoethyl)-2-(6-methoxy-2-naphthyl)-1,3-dioxolane-4(R),5(R)-dicarboxylic acid 5 and 6 (16 g, 0.0367 mol; yield 85.5%) in ratio 5:6=1:1 (determined by 1H-NMR 200 MHz).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04734507uspto-grants-1988_03