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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883988Generated: November 2, 2026

HCID 23507944, compound → HCID 23507950, compound

https://huagongshe.com/reaction/1883988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23507944HCID 23507944—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23507950HCID 2350795046.7%

Reaction Steps

A solution of 7′-ethynyl-3′,4′-dihydrospiro[1,3-dioxolane-2,2′(1′H)naphthalene] (0.85 g, 3.9 mmol) in THF (15 ml) and 1N HCl (5 ml) was stirred overnight at room temperature. Concentrated HCl (2×0.5 ml) was then added in two aliquots 2 hours apart. After stirring a further 2 hours the solution was diluted with diethyl ether, the aqueous phase was separated, and the solution dried (MgSO4) and concentrated in vacuo. The residue was purified by chromatography on silica gel (15 g) eluting with diethyl ether:hexane (1:9→1:4) to give 7-ethynyl-2-tetralone as a solid (0.31 g). 1H NMR (CDCl3, 200 MHz) δ: 2.54 (t, J=7 Hz, 2H, CH2), 3.05 (s, 1H, ethynylH), 3.06 (t, J=7 Hz, 2H, CH2), 3.56 (s, 2H, CH2), 7.18 (d, J=8 Hz, 1H, Ar), 7.26 (s, 1H, Ar), 7.34 (d, J=8 Hz, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762188B1
Source datasetuspto-grants-2004_07
ORD IDord-c112eacab04541afb6b1b737a4944727
Source noteuspto-grants-2004_07