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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680320Generated: October 30, 2026

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

https://huagongshe.com/reaction/1680320

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 numberUS04272437
Source datasetuspto-grants-1981_06
ORD IDord-c7e826a1810b48fb816e9f3f8f9bb92d
Source noteuspto-grants-1981_06