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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-phenoxy-2H-1-benzopyran | HCID 19815615 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-phenoxy-2H-1-benzopyran-3-carboxaldehyde | HCID 14971265 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05155130 |
|---|
| Source dataset | uspto-grants-1992_10 |
|---|
| ORD ID | ord-d06081969dae465aaa28a5bee1c87b47 |
|---|
| Source note | uspto-grants-1992_10 |
|---|