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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640426Generated: October 31, 2026

Benzaldehyde → HCID 178526885, compound

https://huagongshe.com/reaction/1640426

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 numberUS08114870B2
Source datasetuspto-grants-2012_02
ORD IDord-79f0d4dcb298416ea79e6aa51e3e8caa
Source noteuspto-grants-2012_02