HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 21270414, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Isopropanol carbon dioxide | HCID 86586944 | — |
| Reactant | HCID 178469471 | HCID 178469471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21270414 | HCID 21270414 | — |
Reaction Steps
Oxalyl chloride (1.82 g) is added to 100 mL of DMF dropwise under stirring and cooling (isopropanol-dry ice) maintaining the temperature below -20°. Stirring is continued for 30 minutes at the same temperature. To the mixture, 2.66 g of ethyl 6-benzyloxycarbonyloxy-4-hydroxy-5,6,7,8-tetrahydroquinoline-3-carboxylate is added in one portion, and stirring is continued for 2 hours at -30° to -20°, then at room temperature overnight. The reaction mixture is evaported to dryness and the residue is taken up in CH2Cl2, washed with saturated NaHCO3, dried (MgSO4) and evaporated to leave an oil which is purified by flash chromatography on a silica gel column obtaining ethyl 6-benzyloxycarbonyloxy-4-chloro-5,6,7,8-tetrahydroquinoline-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04740512 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-edd69df76f434880b8643753b3097abc |
| Source note | uspto-grants-1988_04 |