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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629767Generated: November 2, 2026

4-Chlorobenzaldehyde → HCID 12157976, compound

https://huagongshe.com/reaction/629767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86726375HCID 86726375—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12157976HCID 1215797674%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (R)-dimethyl 2-oxo-2-(2-oxo-4-phenyloxazolidin-3-yl)ethylphosphonate (60.7 g, 177.8 mmol) in dry THF (275 ml) under an atmosphere of N2 was cooled to 0° C. in an ice-water bath. Potassium tert-butoxide (23.9 g, 213.4 mmol, 1.0 M solution in THF) was added over a period of 45 min in a dropwise manner and the reaction mixture stirred at 0° C. for 30 min. A solution of 4-chlorobenzaldehyde (25.0 g, 177.84 mmol) in dry THF (100 ml) was added over a period of 20 min and the reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was cooled to 0° C. and quenched with saturated solution of ammonium chloride (250 mL) and diluted with EtOAc (1.5 L). The biphasic system was stirred at ambient temperature for 10 min and the layers were separated. The organic layer was washed with brine (250 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by SiO2 column using a gradient elution of 0-25% EtOAc in hexanes. Fractions containing product were combined and the solvents were removed in vacuo to provide the product (43.0 g, 74%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-066cf1545e3649509cfeb9d50a94beb1
Source noteuspto-grants-2016_04