Ethyl chloroformate → 1-Ethoxycarbonyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidine

HRID 2232331Notes

Reaction equation

HRID 2232331 reaction equation
C[N:2]1[CH2:7][CH2:6][C:5]([C:19]#[CH:20])([O:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=2[N+:16]([O-:18])=[O:17])[CH2:4][CH2:3]1.C(=O)([O-])[O-].[K+].[K+].Cl[C:28]([O:30][CH2:31][CH3:32])=[O:29]>C1C=CC=CC=1>[CH2:31]([O:30][C:28]([N:2]1[CH2:7][CH2:6][C:5]([C:19]#[CH:20])([O:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=2[N+:16]([O-:18])=[O:17])[CH2:4][CH2:3]1)=[O:29])[CH3:32]

Participants

5

Procedure

A suspension of 223 g of N-methyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidine, 2 l of dry benzene, 165 g of anhydrous potassium carbonate and 130.3 g of ethyl chloroformate was stirred at reflux for 18 hr under nitrogen. The mixture was filtered and the solvent evaporated. The residue was dissolved in ether, washed with hydrochloric acid, saturated sodium bicarbonate solution, water and saturated sodium chloride solution. The ether solution was dried over anhydrous sodium sulfate and filtered. Evaporation of solvent provided an oil, which was dried at 50°-55° (1 mm). The oil crystallized to provide 226 g (83.8%) of product, mp 56°-68°.

Workup

  1. temperatureat reflux for 18 hr under nitrogen
  2. filtrationThe mixture was filtered
  3. customthe solvent evaporated
  4. dissolutionThe residue was dissolved in ether
  5. washwashed with hydrochloric acid, saturated sodium bicarbonate solution, water and saturated sodium chloride solution
  6. dry with materialThe ether solution was dried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. customEvaporation of solvent
  9. customprovided an oil, which
  10. customwas dried at 50°-55° (1 mm)
  11. customThe oil crystallized

Sources & evidence

ORD record
ord-41fdc70151b14ee6acd1e800ec3fe806
Source dataset
uspto-grants-1988_11
Patent number
US04788201

Reaction notes

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