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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417929Generated: November 3, 2026

Triphenylphosphine → HCID 178520709, compound

https://huagongshe.com/reaction/1417929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl 4-bromo-but-2-enateHCID 54298885—
SolventBenzeneHCID 241—
ProductHCID 178520709HCID 17852070959%

Reaction Steps

A solution of benzyl 4-bromo-but-2-enate (430 mg, 1.68 mmol) and triphenylphosphine (661 mg, 2.52 mmol) in benzene (3 ml) was stirred at room temperature under nitrogen for 20 hours. The resulting white solid was collected through filtration and washed with benzene (3×2 ml), and dried at 100° C. under vacuum to give the title compound (510 mg, 59% yield). 1H NMR (CD3OD): δppm 4.60 (2H, m, slowly disappeared due to deuterium exchange), 5.13 (2H, s), 6.16 (1H, dd, J1=15.3 Hz, J2=1.1 Hz), 6.81 (1H, m), 7.33 (5H, m), 7.78 (12 H, m), 7.90 (3H, m). 13C NMR (CD3OD): δppm 67.6 (t), 68.1 (t), 118.3 (s), 118.8 (s), 119.4 (s), 120.0 (s), 129.3 (d), 129.4 (d), 129.5 (d), 129.6 (d), 129.7 (d), 131.4 (d), 131.5 (d), 131.7 (d), 134.7 (d), 134.85 (d), 134.94 (d), 135.1 (d), 135.2 (d), 135.3 (d), 136.5 (d), 136.6 (d), 136.69 (d), 136.73 (d), 155.7 (s); 165.8 (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05879894
Source datasetuspto-grants-1999_03
ORD IDord-9830221b11fa4aef9e2400df4785e888
Source noteuspto-grants-1999_03