Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848618Generated: October 29, 2026

Ethyl Bromide → HCID 12773961, compound

https://huagongshe.com/reaction/848618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
ReactantMagnesiumHCID 5462224—
Reactant2-Hexenyl bromideHCID 10374753—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12773961HCID 1277396173.3%

Reaction Steps

To a solution of magnesium metal (8.6 g) in dry tetrahydrofuran (100 ml) was added dropwise ethyl bromide (39 g) in a nitrogen atmosphere at ambient temperature. After the mixture was stirred for an hour at the same temperature, to the mixture was added dropwise a solution of 3-(2-tetrahydropyranyloxy)-1-propyne (50 g) in dry tetrahydrofuran (75 ml) and cuprous cyanide (20 mg). The reaction mixture was stirred for 30 minutes at ambient temperature. To the mixture was added with stirring a solution of 1-bromo-trans-2-hexene (58 g) in dry tetrahydrofuran (75 ml) under ice-cooling. The reaction mixture was stirred for 30 minutes at ambient temperature and concentrated under reduced pressure to give a residue, which was dissolved in diluted hydrochloric acid and extracted with ether. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give a yellowish oily residue, which was distilled under reduced pressure to give colorless oily 1-(2-tetrahydropyranyloxy)-trans-5-nonen-2-yne (58 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297096
Source datasetuspto-grants-1981_10
ORD IDord-77e7b4971bf14f21b1ce29c5b3231860
Source noteuspto-grants-1981_10