HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289231Generated: October 30, 2026
Trimethylsilylacetylene → HCID 23507984, compound
https://huagongshe.com/reaction/2289231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | HCID 23507886 | HCID 23507886 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 23507984 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090941 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-afc05c523ca74837be8f0c66a79524d5 |
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| Source note | uspto-grants-2000_07 |
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