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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946953Generated: November 1, 2026

1-Phenyl-1-propanone → HCID 66625783, compound

https://huagongshe.com/reaction/1946953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-1-propanoneHCID 7148—
Reactantdiethyl ((1-(triphenylmethyl)-1H-imidazol-4-yl)methyl)phosphonateHCID 2763175—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 66625783HCID 66625783—

Reaction Steps

To a stirred solution of (1-trityl-1H-imidazol-4-ylmethyl)-phosphonic acid diethyl ester (1.24 g; CAS 473659-21-1) at room temperature (r.t.) in THF (20 ml) under an argon atmosphere was added potassium tert-butylate (301 mg). After 15 minutes stirring at room temperature, propiophenone (0.3 ml) was added in one portion. The mixture was heated to 80° C. and stirring at that temperature was continued for 2 days. The compact suspension was cooled to r.t. and the solid was filtered off and washed with THF. The filtrate was concentrated to leave a dark violet viscous oil. This was taken up in ethyl acetate (EtOAc) and washed with brine. The aqueous phase was back extracted with EtOAc. The combined organics were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (silica gel; gradient cyclohexane→cyclohexane/EtOAc 3:2) to give 4-(2-phenyl-but-1-enyl)-1-trityl-1H-imidazole (269 mg; not completely pure) as an off-white solid. MS (ISP): 243.2 ([Trt]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399463B2
Source datasetuspto-grants-2013_03
ORD IDord-9610251b7ea44607a0f311605ab5e231
Source noteuspto-grants-2013_03