تفاعل #1365700

ord-2aa132d7e98c4a0ea35b10fc28db711d

معادلة التفاعل

[Na+].[OH-]
NaOH
[Al+3].[H-].[H-].[H-].[H-].[Li+]
LiAlH4
CCOC(=O)[C@@H]1C(=O)N(C)C(=O)C[C@H]1c1ccc(F)cc1
(+/−) trans-3-ethoxycarbonyl-4-(4′-fluorophenyl)-N-methyl-piperidine-2,6-dione
Cc1ccccc1
toluene
CN1CC[C@@H](c2ccc(F)cc2)[C@H](CO)C1
(+/−) trans-4-(4′-fluorophenyl)-3-hydroxymethyl-N-methylpiperidine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    أخرىAfter 30 minutes at room temperature reaction
  3. 3
    درجة الحرارةwas heated to >40° C. for 2 hr
  4. 4
    أخرىReaction
  5. 5
    درجة الحرارةwas then cooled to <5° C.
  6. 6
    أخرىthe temperature below 15° C
  7. 7
    أخرىThe solid inorganic salts were removed by filtration
  8. 8
    غسيلThese solids were washed with additional THF or toluene
  9. 9
    تركيزThe filtered solution was then concentrated

الإجراء التجريبي

To a cooled solution of LiAlH4 (0.22 mol) in toluene/THF under argon was added (+/−) trans-3-ethoxycarbonyl-4-(4′-fluorophenyl)-N-methyl-piperidine-2,6-dione (0.083 mol) in THF holding the temperature below 15° C. After addition was complete, the reaction was allowed to warm to room temperature. After 30 minutes at room temperature reaction was heated to >40° C. for 2 hr. Reaction was then cooled to <5° C. and toluene (50 ml) was added. Water (9 ml) was then added slowly holding the temperature below 15° C. Additional H2O or aqueous NaOH was used as necessary. The solid inorganic salts were removed by filtration. These solids were washed with additional THF or toluene. The filtered solution was then concentrated to give (+/−) trans-4-(4′-fluorophenyl)-3-hydroxymethyl-N-methylpiperidine in higher yield (but similar impurity profile) as with NaAlH4 as shown by HPLC analysis. The product can be recovered by standard procedures such as trituration with a less polar solvent.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06444190B2uspto-grants-2002_09