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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297927Generated: October 31, 2026

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

https://huagongshe.com/reaction/2297927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantCbz-L-PhenylalaninalHCID 7021150—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product2-Benzyloxycarbonylamino-1-phenyl-3-buteneHCID 13606586—

Reaction Conditions

Temperature-78 °C

Reaction Steps

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° 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492400B1
Source datasetuspto-grants-2002_12
ORD IDord-6b357624157743b3a118626c090e24e3
Source noteuspto-grants-2002_12