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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294522Generated: October 27, 2026

Formic Acid → Adenine

https://huagongshe.com/reaction/2294522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
Reactant5-Nitroso-4,6-pyrimidinediamineHCID 259752—
ReactantSodium FormateHCID 2723810—
CatalystPalladiumHCID 23938—
SolventFormamideHCID 713—
ProductAdenineHCID 19090%

Reaction Steps

13.9 g (0.1 mol) 4,6-diamino-5-nitrosopyrimidine was suspended in 50 ml formamide, 6.8 g (0.1 mol) sodium formate, 27.0 g (0.5 mol) 85% formic acid and 0.5 g palladium catalyst were added according to example 1 and the mixture was heated for 4 hours to 110° C. The decolorized suspension was subsequently heated for 3 hours to 180° C. and then cooled. In order to improve the processing, 50 ml water was added and the solid was filtered. The filter cake was dissolved in 160 ml 5% sodium hydroxide solution and the insoluble Pd catalyst was separated. The clear filtrate was adjusted with sulphuric acid to a pH value of 8.5 after a 30 minute treatment at 50° C. with 3 g active carbon. In this process a colorless precipitate separated out from adenine which was suction filtered, washed twice with 30 ml water and dried in a vacuum at 80° C. 12.2 g adenine (0.090 mol, 90% of theory) was obtained in this way as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688947
Source datasetuspto-grants-1997_11
ORD IDord-6ca92aea4b424904b29b5ab7c0d216bd
Source noteuspto-grants-1997_11