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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706371Generated: November 1, 2026

Ethyl Bromide → HCID 20335668, compound

https://huagongshe.com/reaction/1706371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13298152HCID 13298152—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 20335668HCID 20335668—

Reaction Steps

20 g of 3-methyl-7-(hex-5-enyl)-xanthine (see Example 22) are added to a solution of approximately 3.3 g of NaOH in 70 ml of methanol/water (1:1) and 9 g of ethyl bromide are added thereto. The mixture is kept at 40° C. under a nitrogen atmosphere for 40 hours. The solvent is then removed under reduced pressure, the residue dissolved in diethyl ether and the pH of the solution is adjusted with aqueous sodium hydroxide solution to a pH-value of 13.5 to remove unreacted 3-methyl-7-(hex-5-enyl)-xanthine. 1-Ethyl-3-methyl-7-(hex-5-enyl)-xanthine recovered from the ether phase is subsequently subjected to column chromatography using silica gel with methylene chloride/acetone (8:2) as eluent followed by distillation under reduced pressure and is obtained as a colourless oil. Yield: 11.2 g (81.3% of theory relative to reacted starting material) of the title compound, nD20 =1.5415.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207321
Source datasetuspto-grants-1980_06
ORD IDord-6d3b893e43f448acbdc25f2c6027bb15
Source noteuspto-grants-1980_06