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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722236Generated: October 26, 2026

Ammonia → 5-(4'Bromophenyl)-4-pentyn-1-al ethylene acetal

https://huagongshe.com/reaction/1722236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantLithium amideHCID 24532—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(2-Bromoethyl)-1,3-dioxolaneHCID 87776—
ReactantBenzene, 1-bromo-4-ethynyl-HCID 136603—
ReactantLithiumHCID 3028194—
SolventDimethyl SulfoxideHCID 679—
Product5-(4'Bromophenyl)-4-pentyn-1-al ethylene acetalHCID 2304932826.4%

Reaction Conditions

Temperature-30 °C

Reaction Steps

4-bromophenylacetylene (10 g, 55 mmol), prepared according to Organic Reactions 5 (1), 50, (1949), in dry dimethyl sulphoxide (70 ml) was added to lithium amide (from 66 mmol) of lithium) in liquid ammonia (200 ml). The mixture was stirred for 1 hour at -30° C., 2-(2-bromoethyl)-1,3-dioxolane (10 g, 55 mmol) was added and the mixture was stirred for 2 hours at -30° C. Ammonium chloride (12 g) was added, the ammonia was allowed to evaporate and water (200 ml) was added to the residue. The emulsion was extracted with ether and the organic phase was washed with brine and dried. The solvents were removed and the product purified by dry column chromatography (silica, 5% ether in hexane 1:1 ether:hexane) to give 4.08 g (26% of theory) of 5-(4'bromophenyl)-4-pentyn-1-al ethylene acetal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855086
Source datasetuspto-grants-1989_08
ORD IDord-e7f7212531b4427cb659861552de10bf
Source noteuspto-grants-1989_08