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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981910Generated: October 25, 2026

Chloride → 3(2-Propynyl)benzaldehyde ethylene acetal

https://huagongshe.com/reaction/1981910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantIodineHCID 807—
Reactant2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
Reactant1-Methoxypropa-1,2-dieneHCID 139403—
CatalystCuprous chlorideHCID 62652—
SolventTetrahydrofuranHCID 8028—
Product3(2-Propynyl)benzaldehyde ethylene acetalHCID 21282857—

Reaction Conditions

Temperature20 °C

Reaction Steps

Dry Mg (0.74 g) under dry N2 in a flask is covered with THF (10 ml) and a crystal of I2 added. 5 ml of a solution of 3-bromobenzaldehyde ethylene acetal (7.0 g) in THF (30 ml) is added and kept until it becomes warm, when it is cooled to 15°, and the remainder of the acetal solution added over 15 minutes, then stirred for an additional 1 hour. A mixture of methoxyallene (2.45 g), copper (1)chloride (0.30 g) and THF (30 ml) is cooled to -20°. The above Grignard solution (under moisture excluding conditions) is then added to this solution during 5 minutes, and allowed to warm to 20° C. with stirring over 30 minutes. Saturated aqueous ammnium chloride is added and the product is extracted with ether. The ether layer is washed with water, dried (MgSO4) and the residue distilled in vacuo. Yield 4.3 g (75%) 89°-96° (0.03 m Hg), nD20 1.5422.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04594355
Source datasetuspto-grants-1986_06
ORD IDord-80d5428756d94e04aea1cbb298067e4d
Source noteuspto-grants-1986_06