Ammonium Chloride → 2-Benzyloxycarbonylamino-1-phenyl-3-butene

HRID 1837005Notes

Reaction equation

HRID 1837005 reaction equation
[CH2:1]([Li])CCC.[C:6]([NH:16][C@H:17]([CH:25]=O)[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:7].[NH4+].[Cl-]>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O1CCCC1>[CH2:9]([O:8][C:6]([NH:16][CH:17]([CH:25]=[CH2:1])[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:7])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

Participants

6

Reactant 3

HCID 25517Ammonium ChlorideHCID 7021150Cbz-L-PhenylalaninalHCID 178418339Butyllithium

Product 1

HCID 136065862-Benzyloxycarbonylamino-1-phenyl-3-butene

Reagents, catalysts & solvents 2

HCID 74505Methyltriphenyliphosphonium bromideCatalystHCID 8028TetrahydrofuranSolvent2×

Procedure

To a stirred suspension of methyltriphenylphosphonium bromide (10.72 g, 0.03 moles) in 100 mL of dry tetrahydofuran at −78° C. was added dropwise 1.6M n-butyl lithium (17.5 mL, 0.028 moles), and the mixture was stirred for 0.5 hrs at −78˜−20° C. Then was added a solution of N-Cbz-phenylalaninal (5.67 g, 0.02 moles) in 50 mL of dry tetrahydrofuran, and the mixture was stirred for 16 hrs at room temperature. After addition of saturated NH4Cl (50 mL) the mixture was extracted with EtOAc, and the extract was washed with water and brine. It was dried over Na2SO4 and evaporated to give an oily residue. The crude product was purified by column chromatograpy on silica gel with elution by 5:95 EtOAc-hexane to give pure 2-benzyloxycarbonylamino-1-phenyl-3-butene.

Workup

  1. stirringthe mixture was stirred for 16 hrs at room temperature
  2. extractionwas extracted with EtOAc
  3. washthe extract was washed with water and brine
  4. dry with materialIt was dried over Na2SO4
  5. customevaporated
  6. customto give an oily residue
  7. customThe crude product was purified by column chromatograpy on silica gel with elution by 5:95 EtOAc-hexane

Sources & evidence

ORD record
ord-4d565dfbef4d492b98d67e46523f7dbf
Source dataset
uspto-grants-2004_08
Patent number
US06780857B2

Reaction notes

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