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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706369Generated: October 25, 2026

Homoallyl bromide → HCID 13298148, compound

https://huagongshe.com/reaction/1706369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomoallyl bromideHCID 21241—
Reactant3,7-Dihydro-1,3-dimethyl-1H-purine-2,6-dione, sodium saltHCID 66973603—
SolventDimethylformamideHCID 6228—
ProductHCID 13298148HCID 13298148—

Reaction Steps

13.9 g of 4-bromo-but-1-ene are reacted with 20.2 g of sodium theophylline in 200 ml of dimethyl-formamide at 120° C. with stirring for approximately 6 to 8 hours until the reaction is complete as indicated by thin-layer chromatography. The solvent is then removed under reduced pressure. The residue is dissolved at 20° C. in 100 ml of methylene chloride, separated from insoluble sodium bromide and purified through a column packed with neutral aluminum oxide to remove small quantities of dark-coloured accompanying substances. Melting point: 110° C. (acetone); yield: 21.6 g (91% of theory relative to the starting material used). After thin-layer chromatography on Merck DC finished plates of silica gel 60 F254 with benzene/acetone (6:4) as eluent, the product has an Rf value of 0.54; and with nitromethane/benzene/pyridine (20:10:3) as eluent, an Rf value of 0.65. Utra-violet light was used as indicator, the pyridine of the eluent having, however, to be removed at 50° C. under reduced pressure because of its property to extinguish fluorescence.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207321
Source datasetuspto-grants-1980_06
ORD IDord-5a5b1dcd0f4a429480a540dbf9f63359
Source noteuspto-grants-1980_06