HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 20556839, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 20556841 | HCID 20556841 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 20556839 | HCID 20556839 | — |
Reaction Steps
To 3.08 g. of 3-phenyl-6-(1,2,3,4-tetrahydro-2-isoquinolyl)-methyl-5,6-dihydro-4H-1,2,4-oxadiazine 50 ml. of absolute acetone, 1.0 ml. of chlorocarbonic acid ethyl ester and 1.0 g. of anhydrous potassium carbonate are added. The reaction mixture is refluxed for 6 hours. The insoluble substances are filtered off while hot and the solvent is evaporated. After recrystallization of the residue from cyclohexane 1.18 g. of 3-phenyl-4-ethoxycarbonyl-6-(1,2,3,4-tetrahydro-2-isoquinolyl)-methyl-5,6-dihydro-1,2,4-oxadiazine are obtained, melting at 114° to 116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04308270 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-5da915989dae4cae9de9090c5dbb715b |
| Source note | uspto-grants-1981_12 |