Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815816Generated: November 2, 2026

Phosphonium, (bromomethyl)triphenyl-, bromide (1:1) → HCID 22144719, compound

https://huagongshe.com/reaction/1815816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphonium, (bromomethyl)triphenyl-, bromide (1:1)HCID 2733422—
ReactantHCID 22144741HCID 22144741—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 22144719HCID 2214471984.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 49.2 gm (0.19 mole) 2-hydroxy-3-bromo-5-fluoro-6-chlorobenzaldehyde and 127 gm (0.29 mole) (bromomethyl)triphenylphosphonium bromide in 230 mL tetrahydrofuran was cooled to 0° C. under a nitrogen atmosphere. To this were added dropwise 330 mL (0.33 mole) potassium tert-butoxide (1M in tetrahydrofuran) over 3 hours. An additional 90 mL (0.09 mole) potassium tert-butoxide (1M in tetrahydrofuran) were then added to react remaining starting material. The reaction mixture was diluted with 700 mL of hexane and the resulting precipitate removed by filtration. The recovered solid was slurried in 300 mL hexane and filtered 4 times. The combined filtrates were washed with 2×500 mL water followed by 500 mL saturated aqueous sodium chloride. The remaining organics were dried over sodium sulfate and concentrated under reduced pressure to provide a residual solid. This solid was slurried and filtered with 4×300 mL diethyl ether to remove triphenylphosphine oxide. The filtrates were concentrated and the residue subjected to silica gel chromatography, eluting with hexane. Fractions containing product were combined and concentrated under reduced pressure to provide 40 gm (83%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881733B1
Source datasetuspto-grants-2005_04
ORD IDord-4f49260b393e401abc274abd55537547
Source noteuspto-grants-2005_04