Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837005Generated: October 30, 2026

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

https://huagongshe.com/reaction/1837005

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 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˜−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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780857B2
Source datasetuspto-grants-2004_08
ORD IDord-4d565dfbef4d492b98d67e46523f7dbf
Source noteuspto-grants-2004_08