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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Cbz-L-Phenylalaninal | HCID 7021150 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzyloxycarbonylamino-1-phenyl-3-butene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06780857B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-4d565dfbef4d492b98d67e46523f7dbf |
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| Source note | uspto-grants-2004_08 |
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