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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289231Generated: October 30, 2026

Trimethylsilylacetylene → HCID 23507984, compound

https://huagongshe.com/reaction/2289231

Reaction equation

Participants

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

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) (Aidrich), triphenyephosphine (0.66 g, 2.50 mmol), and palladium acetate (0.28 g, 1.2 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 numberUS06090941
Source datasetuspto-grants-2000_07
ORD IDord-afc05c523ca74837be8f0c66a79524d5
Source noteuspto-grants-2000_07