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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764118Generated: November 3, 2026

3-Nitrobenzaldehyde → HCID 20306576, compound

https://huagongshe.com/reaction/1764118

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
Reactant3,4-Dihydro-2H-1-benzopyran-4-amineHCID 4961957—
SolventEthanolHCID 702—
ProductHCID 20306576HCID 20306576—

Reaction Steps

An 80 g, (0.54 mole) portion of 4-chromanamine, and 650 ml of ethanol were placed in a 2-l, 3-necked flask, equipped with a stirrer and reflux condenser fitted with a drying tube. The slurry was treated with 85 g (0.56 mole) portion of m-nitrobenzaldehyde using rapid mechanical stirring. The reaction mixture was refluxed for 5 hrs., cooled 1 hr. and filtered. The yellow crystalline solid was washed with 100 ml of ethanol, ether, and dried, m.p. 117°-118°. Yield: 115 g (76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115407
Source datasetuspto-grants-1978_09
ORD IDord-af9017eba49b4999841395986d2365b4
Source noteuspto-grants-1978_09