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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24233Generated: October 29, 2026

Triphenylphosphine → Ethyl4-(4-bromomethyl-3-methyl-phenylethynyl)-benzoate

https://huagongshe.com/reaction/24233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22568788HCID 22568788—
SolventDichloromethaneHCID 6344—
ProductEthyl4-(4-bromomethyl-3-methyl-phenylethynyl)-benzoateHCID 22568891—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of ethyl 4-(4-hydroxymethyl-3-methyl-phenylethynyl)-benzoate (Compound 117, 130.0 mg, 0.44 mmol) and triphenylphosphine (150.0 mg, 0.57 mmol) in 5 mL CH2Cl2 was cooled to 0° C. and N-bromosuccinimide (101.0 mg, 0.57 mmol) was added in 5 portions over 20 minutes. The solution was warmed to 25° C. and stirred for 17 hours. The reaction was quenched by the addition of dilute aqueous NaHCO3. The resulting mixture was extracted with Et2O and the combined organic layers were washed with H2O and saturated aqueous NaCl before being dried (Na2SO4) and concentrated under reduced pressure. The title compound, 120.0 mg (76%), was isolated by column chromatography (2-5% EtOAc—hexanes) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855512B2
Source datasetuspto-grants-2005_02
ORD IDord-0e7e0a2541644682a092a5bac7d1fcc8
Source noteuspto-grants-2005_02