Methanol → Ethyl 4-hydroxypiperidine-1-carboxylate

HRID 2309608Notes

Reaction equation

HRID 2309608 reaction equation
[O:1]=[C:2]1[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]1.CO.[BH4-].[Na+].[Cl-].[NH4+]>O>[OH:1][CH:2]1[CH2:3][CH2:4][N:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:6][CH2:7]1

Participants

6

Procedure

To a suspension of 68.5 parts of ethyl 4-oxo-1-piperidinecarboxylate in 240 parts of methanol were added portionwise 3.8 parts of sodium borohydride at a temperature between 20°-30° C. (the reaction mixture was cooled if necessary in a water bath). After the addition was complete, the whole was stirred for 30 minutes. The reaction mixture was then poured into a mixture of 53.5 parts of ammonium chloride and 400 parts of water. The methanol was evaporated. The product was extracted with trichloromethane. The extract was dried and evaporated. The oily residue was distilled in vacuo, yielding 60 parts of oily ethyl 4-hydroxy-1-piperidinecarboxylate; bp. 140° C. at 1.4 mm. pressure; nD20 : 1.4796; d2020 : 1.1166 (3).

Workup

  1. temperaturewas cooled if necessary in a water bath)
  2. additionAfter the addition
  3. customThe methanol was evaporated
  4. extractionThe product was extracted with trichloromethane
  5. customThe extract was dried
  6. customevaporated
  7. distillationThe oily residue was distilled in vacuo

Sources & evidence

ORD record
ord-9b6d5979f0494862af1b4e02c47c59f8
Source dataset
uspto-grants-1987_09
Patent number
US04695575

Reaction notes

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