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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381546Generated: October 31, 2026

Triphenylphosphine → HCID 23507984, compound

https://huagongshe.com/reaction/381546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 23507886HCID 23507886—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
ProductHCID 23507984HCID 2350798440.2%

Reaction Steps

A solution of 7′-bromo-3′,4′-dihydrospiro[1,3-dioxolane-2,2′(1H)-naphthalene] (3.40 g, 12.6 mmol), trimethylsilylacetylene (7.0 ml, 50 mmol) (Aldrich), triphenylphosphine (0.66 g, 2.50 mmol), and palladium acetate (0.28 g, 1.25 mmol) in triethylamine (18 ml) was stirred at 70° C. for 18 hours and then concentrated in vacuo. The residue was absorbed onto silica gel from a diethyl ether solution and partially purified by elution through silica gel (15 g) with diethyl ether: hexane (1:9). Further purification by chromatography on silica gel eluting with ethyl acetate:hexane (1:19) gave 3′,4′-dihydro-7′[2-(trimethylsilyl)ethynyl]spiro[1,3-dioxolane-2,2′(1′H)-naphthalene] (1.45 g). 1H NMR (CDCl3 200 MHz) δ: 0.23 (s, 9H, SiMe3), 1.93 (t, J=7 Hz, 2 CH2), 2.95 (t, J=7 Hz, 2H, CH2), 4.02 (s, 4H, OCH2CH2O), 7.03 (d, J=8 Hz, 1H, Ar), 7.17 (s, 1H, Ar), 7.21 (d, J=8 Hz, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306865B1
Source datasetuspto-grants-2001_10
ORD IDord-044bade44fc04af89396d3d5d8e2af7d
Source noteuspto-grants-2001_10