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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229328Generated: October 30, 2026

Benzaldehyde → HCID 178526885, compound

https://huagongshe.com/reaction/229328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethanolHCID 887—
ReactantPiperidineHCID 8082—
ReactantHCID 178433493HCID 178433493—
SolventDiethyl EtherHCID 3283—
ProductHCID 178526885HCID 17852688563.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-methyl-5-nitropyrimidine-4,6-diol (4.7 g, 27.5 mmol) and benzaldehyde (42 mL, 414 mmol) was treated with piperidine (21.3 mL, 215.3 mmol). The reaction mixture was heated to 90° C. for 2 hrs. The temperature was then increased to 120° C. for 30 min. After cooling the reaction mixture to ambient, methanol (10 mL) and diethyl ether (200 mL) were added sequentially. The resulting solid was collected by filtration and washed with 5% aqueous hydrochloric acid to give 5-nitro-2-[(E)-2-phenylvinyl]pyrimidine-4,6-diol (4.5 g). 1H NMR (400 MHz, DMSO-d6): δ 8.15 (d, 1H, J=16.4 Hz), 7.15 (m, 2H), 7.54 (m, 3H), 6.81 (d, 1H, J=16.4 Hz). MS (m/z) 260 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563787B2
Source datasetuspto-grants-2009_07
ORD IDord-c47d854b77324958bc884afeafa69622
Source noteuspto-grants-2009_07