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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466190Generated: October 30, 2026

Ammonium Hydroxide → 6-phenoxy-2H-1-benzopyran-3-carboxaldehyde

https://huagongshe.com/reaction/466190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantN-FormylmorpholineHCID 20417—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-phenoxy-2H-1-benzopyranHCID 19815615—
SolventDichloromethaneHCID 6344—
Product6-phenoxy-2H-1-benzopyran-3-carboxaldehydeHCID 14971265—

Reaction Conditions

Temperature60 °C

Reaction Steps

6-Phenoxy-2H-1-benzopyran (3.36 g, 15 mmol) and N-formylmorpholine (10.4 g, 90 mmol) are dissolved in 10.5 ml of methylene chloride and treated with phosphorus oxychloride (13.8 g, 90 mmol) at 0° C. over 15 minutes. The mixture is then heated at 60° C. for 27 hours, cooled and poured slowly into an ice-water mixture. The mixture is then neutralized with aqueous ammonium hydroxide, and extracted twice with methylene chloride. The combined organic extracts are washed with water, dried (MgSO4), and evaporated to give crude 6-phenoxy-2H-1-benzopyran-3-carboxaldehyde, which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155130
Source datasetuspto-grants-1992_10
ORD IDord-d06081969dae465aaa28a5bee1c87b47
Source noteuspto-grants-1992_10