HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → HCID 86742039, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 13316805 | HCID 13316805 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86742039 | HCID 86742039 | — |
Reaction Steps
A mixture of 0.2 g of 5-benzyloxy-β-carboline-3-phosphonic acid diethyl ester (example 61) and 0.1 g of oxalyl chloride in 10 ml of dichloromethane is stirred for 24 hours at room temperature and then mixed with an excess of diethylamine. It is heated to boiling for 2 more hours for completion of the reaction. It is diluted with acetic acid and extracted with water. The evaporation residue of the organic phase yields 0.15 g of the title compound after crystallization from tetrahydrofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731358 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-0644e58133d8430285fc7b778fdd087d |
| Source note | uspto-grants-1988_03 |