Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355213Generated: October 28, 2026

2,6-Lutidine → p-Nitrobenzyl 2-(4-Acetylthio-2-oxo-1-azetidinyl)-2-triphenylphosphoranylideneacetate

https://huagongshe.com/reaction/355213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantTriphenylphosphineHCID 11776—
Reactantp-Nitrobenzyl 2-(4-Acetylthio-2-oxo-1-azetidinyl)-2-chloroacetateHCID 13132062—
Solvent1,4-DioxaneHCID 31275—
Productp-Nitrobenzyl 2-(4-Acetylthio-2-oxo-1-azetidinyl)-2-triphenylphosphoranylideneacetateHCID 13132063—

Reaction Steps

2,6-Lutidine (2.14 g., 20 mmole) was added to a solution of p-nitrobenzyl 2-(4-acetylthio-2-oxo-1-azetidinyl)-2-chloroacetate (5.9 g., 16 mmole) and triphenylphosphine (5.8 g., 22 mmole) in dioxane (80 ml.). The solution was kept at 55° for 18 hours and then concentrated on a rotary evaporator. The residue was partitioned between brine and ethyl acetate and the organic phase was washed with brine, dried and concentrated. The residue was purified by chromatography over silica gel (ethyl acetate:petroleum ether, 1:2 v/v) to give 4.64 g. (48%) of the title ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04378314
Source datasetuspto-grants-1983_03
ORD IDord-2f791f4cf9c84915973838eaa26281e2
Source noteuspto-grants-1983_03