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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285574Generated: October 30, 2026

p-Toluenesulfonic acid → Acyclovir

https://huagongshe.com/reaction/2285574

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,3-DioxolaneHCID 12586—
ReactantDiacetylguanineHCID 136360183—
SolventTolueneHCID 1140—
ProductAcyclovirHCID 13539851321.6%

Reaction Steps

To a mixture of acetic anhydride (1.2 ml) and p-toluenesulfonic acid (0.09 g) was added with stirring dioxolane (1.02 g)-caution, exothermic. The solution was allowed to cool for several minutes. Diacetylguanine (1.45 g) and dry toluene (9 ml) were added and the reaction mixture was stirred at reflux for 18 hr. and then allowed to cool to room temperature. The toluene was decanted off and the residue triturated several times with benzene. Methanol (10 ml) was added to the residue and evaporated under reduced pressure. To the residue was added 40% aqueous methylamine (10 ml) and the mixture heated on a steam bath for 20 min. The water and methylamine were removed under reduced pressure, ethanol (10 ml) was added and evaporated. The residue was thoroughly extracted with boiling methanol (700 ml total) and the combined extracts evaporated. The resulting solid was triturated with cold ethanol and then recrystallized from methanol to give 9-(2-hydroxyethoxymethyl)guanine (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04323573
Source datasetuspto-grants-1982_04
ORD IDord-8094654c486f4072b4e38455c3916295
Source noteuspto-grants-1982_04