تفاعل #2387327

ord-c8fcbd16c4f94cdcb57e9f9718a69561

معادلة التفاعل

O=C(OCc1ccccc1)N1CCC2(CC1)CO2
benzyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate
O=C([O-])O.[Na+]
sodium bicarbonate
F.c1ccncc1
hydrogen fluoride pyridine
O=C(OCc1ccccc1)N1CCC(F)(CO)CC1
title compound
O=C(OCc1ccccc1)N1CCC(F)(CO)CC1
Benzyl 4-Fluoro-4-hydroxymethyl-1-piperidinecarboxylate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas cooled
  2. 2
    درجة الحرارةcooling
  3. 3
    أخرىThe organic layer was recovered
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    أخرىThe filtrate was evaporated

الإجراء التجريبي

A mixture of 5 ml hydrogen fluoride pyridine and 20 ml methylene chloride was cooled, and 10 ml solution of 4.95 g of benzyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate in methylene chloride was added dropwise thereinto over 25 min such that the bulk temperature was 0° C. or less. The mixture was stirred for 35 min under ice-cooling. The reaction solution was poured into a mixture of saturated sodium bicarbonate and ice. The organic layer was recovered, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated, and then subjected to silica gel column chromatography to give 2.84 g of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06498159B1uspto-grants-2002_12