Sulfuric Acid → Tert-butyl Piperidine-4-carboxylate

HRID 2386105Notes

Reaction equation

HRID 2386105 reaction equation
[NH:1]1[CH2:9][CH2:8][CH:4]([C:5]([OH:7])=[O:6])[CH2:3][CH2:2]1.S(=O)(=O)(O)O>O1CCOCC1>[NH:1]1[CH2:9][CH2:8][CH:4]([C:5]([O:7][C:4]([CH3:8])([CH3:5])[CH3:3])=[O:6])[CH2:3][CH2:2]1

Participants

4

Conditions

Temperature
0 °C

Procedure

To isonipecotic acid (41.5 g; 320 mmol) was added 1,4-dioxane (200 mL). Thus, an inhomogeneous solution was obtained. Thereto was added 41.5 mL of concentrated sulfuric acid over 30 minutes. Into this inhomogeneous solution was bubbled 100 g of isobutene over 5 hours. After completion of the bubbling, the mixture was cooled to 0° C. and 750 mL of 2-N aqueous NaOH solution was added thereto. The resultant mixture was ascertained to be basic. Thereafter, a reaction product was extracted with 500 mL of diethyl ether, and the extract was dried with sodium sulfate and then concentrated to obtain 5.98 g of t-butyl isonipecotate as the target compound.

Workup

  1. customThus, an inhomogeneous solution was obtained
  2. customInto this inhomogeneous solution was bubbled 100 g of isobutene over 5 hours
  3. addition750 mL of 2-N aqueous NaOH solution was added
  4. extractionThereafter, a reaction product was extracted with 500 mL of diethyl ether
  5. dry with materialthe extract was dried with sodium sulfate
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-de4489d1843943fa882b9f8e89cee821
Source dataset
uspto-grants-2012_09
Patent number
US08268402B2

Reaction notes

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