Tetrahydrofuran → Butyl (2-fluorophenyl)carbamate

HRID 619967Notes

Reaction equation

HRID 619967 reaction equation
[F:1][C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].[C:9](=[O:20])([O:15][C:16]([CH3:19])(C)C)OC(C)(C)C.[CH2:21]1COC[CH2:22]1>>[CH2:16]([O:15][C:9]([NH:4][C:3]1[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=1[F:1])=[O:20])[CH2:19][CH2:21][CH3:22]

Participants

4

Reactant 3

HCID 8028TetrahydrofuranHCID 95842-FluoroanilineHCID 10219638Carbonic acid, bis(1,1-dimethylethyl) ester

Product 1

HCID 1562695Butyl (2-fluorophenyl)carbamate

Procedure

A solution of 2-fluoroaniline (30.0 g, 0.27 mol) and di-t-butyl carbonate (66.5 g, 0.30 mol) in 100 ml of THF was heated at reflux for 4 hours. The solvent was removed by evaporation at reduced pressure, and the residue was partitioned between 1M aqueous citric acid and ethyl acetate. The organic phase was washed with saturated aqueous NaCl. The solvent was removed to afford the desired product, which was used without further purification. IR and 1H NMR spectra were in agreement with the assigned structure.

Workup

  1. temperatureat reflux for 4 hours
  2. customThe solvent was removed by evaporation at reduced pressure
  3. customthe residue was partitioned between 1M aqueous citric acid and ethyl acetate
  4. washThe organic phase was washed with saturated aqueous NaCl
  5. customThe solvent was removed

Sources & evidence

ORD record
ord-cca2381b651747009bc059124278a8e8
Source dataset
uspto-grants-1989_04
Patent number
US04818273

Reaction notes

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