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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986545Generated: October 29, 2026

1-Tridecyne → HCID 53669740, compound

https://huagongshe.com/reaction/986545

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-TridecyneHCID 117754—
Reactant2-Propenoic acid, 3-(4-bromophenyl)-, methyl esterHCID 816773—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
ProductHCID 53669740HCID 5366974047%

Reaction Steps

To a deaerated solution of methyl 4-bromocinnamate (9.64 g, 40 mmole) in dry triethylamine (120 ml) was added triphenylphosphine (308 mg) followed by 1-tridecyne (8.00 g, 45 mmole) and palladium (II) acetate (92 mg) under nitrogen. The mixture was heated to reflux for 24 hours, the reaction being followed by hplc. After this time the mixture was cooled and the precipitated triethylamine hydrobromide was filtered off and washed with a little triethylamine. The filtrate was evaporated to a red solid which was chromatographed on 220 g of silica eluting with petroleum ether [bp 60-80]-dichloromethane (3:2) to give 6.26 g (47%) of title compound as a pale yellow solid of mp (MeOH) 57°-59° C., υmax (mull) 1710, 1630, 1600, 1315, 1170, 1000, 830 cm-1, δ(CDCl3). 0.85 (3H, distorted t, terminal CH3), 1.28 (18H, m, alkylene chain), 2.38 (2 H, t, J 6.5 Hz, C≡C--CH2), 3.78 (3H, s, ester CH3), 6.37 (1H, d, J 16 Hz, =CHCO2), 7.42 (4H, near s, arom), 7.63 (1H, d, J 16 Hz, ArCH=)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04713486
Source datasetuspto-grants-1987_12
ORD IDord-56e8b5ed1ac340ea9a19c868ed210814
Source noteuspto-grants-1987_12