HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Trans-6-cyano-4-(ethoxycarbonylamino)-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | (3S,4R)-4-amino-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile | HCID 10943936 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Trans-6-cyano-4-(ethoxycarbonylamino)-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol | HCID 15634874 | — |
Reaction Steps
To trans-4-amino-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol (1.09 g) and triethylamine (0.77 ml) in dichloromethane (20 ml), cooled in an ice bath, was added ethylchloroformate (0.67 ml). The mixture was allowed to attain room temperature and stirred for 2 days. The reaction mixture was washed with water and dried over anhydrous magnesium sulphate. Filtration and evaporation and chromatography (chromatotron, gradient elution: 10-30% Ethyl acetate-pentate) gave one fraction (456 mg) which was recrystallised from ethyl acetate-pentane to give the compound of this example (319 mg); mp 147°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04575511 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-20c66d109ee9412f84ce5aa899090ca0 |
| Source note | uspto-grants-1986_03 |