HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-(1-Hydroxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(3-Cyano-4-oxo-4H-1-benzopyran-6-yl)ethyl acetate | HCID 20358220 | — |
| Product | 6-(1-Hydroxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile | HCID 13601325 | — |
Reaction Steps
A mixture of 1.43 parts of 6-(1-acetoxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile and 25 parts by volume of 1N-sodium hydroxide is stirred at room temperature for 80 minutes. After being acidified with 1N-hydrochloric acid, the reaction mixture is extracted with ethyl acetate. The ethyl acetate layer is washed with water and dried on Na2SO4. The ethyl acetate is distilled off and the resulting residue is recrystallized from ethyl acetate. The procedure yields 0.790 part of 6-(1-hydroxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile as colorless crystals. Melting point: 147°-148° C
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04085116 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-c05b85cbfad3416685ecc796ca9bc821 |
| Source note | uspto-grants-1978_04 |