Ethyl chloroformate → [1-(4-Benzyloxy-3-ethoxy-phenyl)-2-phenyl-ethyl]-(2,2-dimethoxy-ethyl)-carbamic acid ethyl ester

HRID 1833228Notes

Reaction equation

HRID 1833228 reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH:15]([NH:26][CH2:27][CH:28]([O:31][CH3:32])[O:29][CH3:30])[CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[C:19](OCC)[CH:18]=2)=[CH:11][C:10]=1[O:33][CH3:34])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:35](=O)([O-])[O-].[K+].[K+].Cl[C:42]([O:44][CH2:45][CH3:46])=[O:43].C(OCC)(=O)C.CCCCCC>O1CCCC1.O.C(OCC)C>[CH2:45]([O:44][C:42](=[O:43])[N:26]([CH:15]([C:12]1[CH:13]=[CH:14][C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:10]([O:33][CH2:34][CH3:35])[CH:11]=1)[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[CH2:27][CH:28]([O:29][CH3:30])[O:31][CH3:32])[CH3:46]

Participants

8

Reactant 4

HCID 10928Ethyl chloroformateHCID 11430Potassium CarbonateHCID 21226206Ethyl acetate hexaneHCID 22048411[1-(4-Benzyloxy-3-methoxy-phenyl)-2-(3-ethoxy-phenyl)-ethyl]-(2,2-dimethoxy-ethyl)-amine

Product 1

HCID 69551024[1-(4-Benzyloxy-3-ethoxy-phenyl)-2-phenyl-ethyl]-(2,2-dimethoxy-ethyl)-carbamic acid ethyl esterYield 59.1%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Procedure

To a stirred solution of [1-(4-benzyloxy-3-methoxy-phenyl)-2-(3-ethoxy-phenyl)-ethyl]-(2,2-dimethoxy-ethyl)-amine (22.2 g, 40 mmol) in tetrahydrofuran (120 mL) and water (60 mL) was added potassium carbonate (9.93 g, 72 mmol) and ethyl chloroformate (4.2 mL, 44 mmol) dropwise.). The mixture was stirred for 1 h at room temperature. The mixture was diluted with diethyl ether (100 mL), and the organic layer was separated. The aqueous phase was extracted with ethyl acetate (3×100 μL) and the combined extracts were washed with saturated aqueous sodium chloride solution (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70–230 mesh, 20% ethyl acetate/hexane) afforded [1-(4-benzyloxy-3-ethoxy-phenyl)-2-phenyl-ethyl]-(2,2-dimethoxy-ethyl)-carbamic acid ethyl ester (12 g, 56% yield in three steps) as a colorless oil.

Workup

  1. customthe organic layer was separated
  2. extractionThe aqueous phase was extracted with ethyl acetate (3×100 μL)
  3. washthe combined extracts were washed with saturated aqueous sodium chloride solution (100 mL)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-4460d546126147d892ca02c0344b78b3
Source dataset
uspto-grants-2006_06
Patent number
US07067529B2

Reaction notes

Loading…