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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381114Generated: October 31, 2026

Allyl bromide → HCID 13035731, compound

https://huagongshe.com/reaction/1381114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178517111HCID 178517111—
SolventDimethylacetamideHCID 31374—
ProductHCID 13035731HCID 13035731—

Reaction Conditions

Temperature80 °C

Reaction Steps

6.9 g (0.037 mol) of 5-oxo-2,3,5,6-tetrahydroimidazo-[1,2-c]-quinazoline in 60 ml of absolute dimethylacetamide were added to 1.75 g (0.058 mol) of an 80% strength suspension of NaH in oil (Schuchardt), after the suspension had been thoroughly stirred twice with 20 ml of n-hexane in each case and the solvent had been decanted, and the mixture was heated to 80° C. for 1 hour. During this process, a clear solution was gradually formed. The solution was cooled, and 4.6 ml (0.053 mol) of allyl bromide were added dropwise. The mixture was then heated to 100° C. for 4 hours. It was concentrated in a rotary evaporator to one third of its volume and was poured onto ice-water. The precipitated product was filtered off under suction and was recrystallised from methanol/water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585772
Source datasetuspto-grants-1986_04
ORD IDord-a97165cfadea437bab4000e7c24131c5
Source noteuspto-grants-1986_04