Hexane → 1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate

HRID 712207

Reaction equation

HRID 712207 reaction equation
[C:1]([CH:3]1[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)#[N:2].[Li+].CC([N-]C(C)C)C.Cl[C:25]([O:27][CH2:28][CH3:29])=[O:26].CCCCCC>C1COCC1>[C:1]([C:3]1([C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)#[N:2]

Participants

6

Conditions

Temperature
-78 °C

Procedure

A solution of tert-butyl 4-cyanopiperidine-1-carboxylate (0.75 g, 3.57 mmol) in THF (25.0 mL) was cooled to −78° C. followed by dropwise addition of LDA (1.8 M in THF, 6.0 mL, 5.35 mmol) and stirred at the same temperature (−78° C.) for 45 min followed by addition of ethyl chloroformate (0.46 g, 4.28 mmol). The temperature of the reaction was slowly raised to rt and left to stir for 6 h. The reaction was then cooled to 0° C. and quenched by drop wise addition of saturated NH4Cl solution (50 mL), extracted with EtOAc (3×100 mL) and the combined organics washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The crude residue was purified over 100-200 M silica-gel using 7% EtOAc:hexane to obtain the product as an orange viscous liquid (0.4 g, 48% yield). MS: 283.14 [M+H]+.

Workup

  1. temperatureThe temperature of the reaction was slowly raised to rt
  2. waitleft
  3. stirringto stir for 6 h
  4. temperatureThe reaction was then cooled to 0° C.
  5. customquenched by drop wise addition of saturated NH4Cl solution (50 mL)
  6. extractionextracted with EtOAc (3×100 mL)
  7. washthe combined organics washed with brine
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe crude residue was purified over 100-200 M silica-gel

Sources & evidence

ORD record
ord-09798f3e46594c668a7a06e7d4b56e82
Source dataset
uspto-grants-2015_11
Patent number
US09181234B2

Linked notes

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