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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414129Generated: October 25, 2026

Iodine → 3(2-Propynyl)benzaldehyde ethylene acetal

https://huagongshe.com/reaction/414129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
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 Steps

Dry Mg (0.74 g) under dry N2 in a flask is covered with THF (10 ml) and a crystal 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° with stirring over 30 minutes. Saturated aqueous ammonium 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 numberUS04789754
Source datasetuspto-grants-1988_12
ORD IDord-e211f82262d5466591bb47f9cc3c9d80
Source noteuspto-grants-1988_12