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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428700Generated: October 29, 2026

4-Nitrobenzaldehyde → HCID 18359235, compound

https://huagongshe.com/reaction/428700

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(4-Nitrophenyl)prop-2-yn-1-olHCID 132905—
ReactantHCID 178462451HCID 178462451—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 18359235HCID 18359235—

Reaction Steps

1-(4-Nitro-phenyl)-2-propyn-1-ol (4.89 mmol) (prepared by the addition of ethynylmagnesium chloride (Aldrich) to 4-nitrobenzaldehyde (Aldrich) according to method A above) was added to 10% H2O in methanol (150 mL) and to this mixture was added zinc dust (44.01 mmol) and ammonium chloride (10.67 mmol). The reaction was heated at reflux for 3 h, at which time the reaction was cooled and the solid was filtered off. The solids were washed extensively with ethyl acetate, and the ethyl acetate and methanol were evaporated in vacuo. The resulting precipitate was filtered off, dried and recrystallized from ethyl acetate/hexane to yield 1-(4-amino-phenyl)-2-propyn-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313310B1
Source datasetuspto-grants-2001_11
ORD IDord-5326109ac8f6446baaadd46dba193eda
Source noteuspto-grants-2001_11