Diisopropylethylamine → Ethyl 1-benzyl-4-fluoropiperidine-4-carboxylate

HRID 1038824Notes

Reaction equation

HRID 1038824 reaction equation
CCN(C(C)C)C(C)C.[Li]CCCC.[CH2:15]([N:22]1[CH2:27][CH2:26][CH:25]([C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH2:24][CH2:23]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.[F:33]N(S(C1C=CC=CC=1)(=O)=O)S(C1C=CC=CC=1)(=O)=O>C1COCC1.CCOC(C)=O>[CH2:15]([N:22]1[CH2:27][CH2:26][C:25]([F:33])([C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH2:24][CH2:23]1)[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1

Participants

7

Conditions

Temperature
-78 °C

Procedure

A flask was charged with DIEA (8.64 mL, 60.6 mmol) and THF (100 mL). The mixture was cooled to about −78° C. followed by the addition of n-BuLi (24.3 mL, 60.6 mmol) over about 5 min. The mixture was warmed to about 0° C. and stirred for about 30 min and then cooled to about −40° C. To the mixture was added a solution of ethyl 1-benzylpiperidine-4-carboxylate (10.0 g, 40.4 mmol, Oakwood) in THF (75 mL) over about 10 min such that the solution is kept between −40 to −30° C. The mixture was stirred for about 1 h at about −10° C. before being cooled to about −78° C. A solution of N-fluoro-N-(phenylsulfonyl)benzenesulfonamide (14.0 g, 44.5 mmol) in THF (75 mL) was added over about 20 min while keeping the mixture between about −65 and −78° C. The mixture was then stirred for about 1 h at about −78° C. The mixture was poured into a separatory funnel containing ice water (30 mL) and EtOAc (30 mL) was added. The aqueous layer was extracted with EtOAc (3×25 mL) and the combined organic extracts were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The resulting mixture was adsorbed onto silica gel and purified by flash silica gel chromatography eluting with hexanes/EtOAc (10:1) to afford ethyl 1-benzyl-4-fluoropiperidine-4-carboxylate (7.13 g, 66%): LC/MS (Table 2, Method h) Rt=2.21 min; MS m/z: 266 (M+H)+.

Workup

  1. temperatureThe mixture was warmed to about 0° C.
  2. temperaturecooled to about −40° C
  3. customis kept between −40 to −30° C
  4. stirringThe mixture was stirred for about 1 h at about −10° C.
  5. temperaturebefore being cooled to about −78° C
  6. customthe mixture between about −65 and −78° C
  7. stirringThe mixture was then stirred for about 1 h at about −78° C
  8. additionThe mixture was poured into a separatory funnel
  9. additionwas added
  10. extractionThe aqueous layer was extracted with EtOAc (3×25 mL)
  11. washthe combined organic extracts were washed with brine
  12. dry with materialdried over anhydrous Na2SO4
  13. filtrationfiltered
  14. concentrationconcentrated under reduced pressure
  15. custompurified by flash silica gel chromatography
  16. washeluting with hexanes/EtOAc (10:1)

Sources & evidence

ORD record
ord-ac7d0fa03fcd4542aa0c1da292601c9f
Source dataset
uspto-grants-2013_10
Patent number
US08551981B2

Reaction notes

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