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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841739Generated: October 29, 2026

Triphenylphosphine → Methyl [4-(4-bromomethyl-3-isopropyl-phenylethynyl)-phenyl]-acetate

https://huagongshe.com/reaction/841739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl [4-(4-hydroxymethyl-3-isopropyl-phenylethynyl)-phenyl]-acetateHCID 86585933—
SolventDichloromethaneHCID 6344—
ProductMethyl [4-(4-bromomethyl-3-isopropyl-phenylethynyl)-phenyl]-acetateHCID 86585936—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of methyl[4-(4-hydroxymethyl-3-isopropyl-phenylethynyl)-phenyl]-acetate (Compound 123, 180.0 mg, 0.56 mmol) and triphenylphosphine (190.0 mg, 0.73 mmol) in 5 mL CH2Cl2 was cooled to 0° C. and N-bromosuccinimide (130.0 mg, 0.73 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, 212.0 mg (98%), was isolated by column chromatography (5-10% EtOAc-hexanes) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369261B1
Source datasetuspto-grants-2002_04
ORD IDord-2684f6b0a9164ea8ba71a7283c203138
Source noteuspto-grants-2002_04