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Hydrochloric Acid → (2-Benzyloxycarbonylamino-ethyl)-phosphonic acid diethyl ester

HRID 1614910
Notes
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Reaction equation

HRID 1614910 reaction equation
Cl.[CH2:2]([O:4][P:5]([CH2:10][CH2:11][NH2:12])(=[O:9])[O:6][CH2:7][CH3:8])[CH3:3].[C:13](Cl)([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14].CCN(C(C)C)C(C)C>C(Cl)Cl.CCOC(C)=O>[CH2:7]([O:6][P:5]([CH2:10][CH2:11][NH:12][C:13]([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14])(=[O:9])[O:4][CH2:2][CH3:3])[CH3:8]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 10387Benzyl chloroformateHCID 81531DiisopropylethylamineHCID 2733596Diethyl (2-aminoethyl)phosphonate

Product 1

HCID 12487964(2-Benzyloxycarbonylamino-ethyl)-phosphonic acid diethyl ester

Reagents, catalysts & solvents 2

HCID 6344
Dichloromethane
Solvent
HCID 8857Ethyl AcetateSolvent

Procedure

The HCl salt of (2-amino-ethyl)-phosphonic acid diethyl ester (4.5 g, 20.7 mmol) was dissolved in CH2Cl2 (100 mL). To this solution was added CBzCl (3.2 mL, 22.7 mmol), followed by iPr2NEt (14.4 mL, 82.8 mmol). The reaction was stirred at room temperature until complete, as determined by TLC (eluent: 100% EtOAc). The reaction was quenched by the addition of saturated NaHCO3. The mixture was then partitioned between CH2Cl2 and H2O. The layers were separated and the organic layer was washed with brine and then dried over Na2SO4. The drying agent was removed by vacuum filtration and (2-benzyloxycarbonylamino-ethyl)-phosphonic acid diethyl ester was isolated from the concentrated filtrate by silica gel column chromatography (EtOAc/hexanes) (5.98 g, 92%).

Workup

  1. customThe reaction was quenched by the addition of saturated NaHCO3
  2. customThe mixture was then partitioned between CH2Cl2 and H2O
  3. customThe layers were separated
  4. washthe organic layer was washed with brine
  5. dry with materialdried over Na2SO4
  6. customThe drying agent was removed by vacuum filtration

Sources & evidence

ORD record
ord-b1d439d00c2d435ab18937b37453f277
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08765722B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes