HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 131725229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 131725228 | HCID 131725228 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131725229 | HCID 131725229 | — |
Reaction Steps
A mixture of the product from Example 9 step (ii) (1.15 g) and oxalyl chloride (1.2 ml) in dichloromethane (100 ml) was treated with 2 drops of dimethylformamide. After 24 hours at room temperature a further aliquot of oxalyl chloride (3.6 ml) was added and the mixture heated under reflux for 48 hours. The solvent was evaporated under reduced pressure. Toluene was added to the residue and then evaporated under reduced pressure to give the subtitle product as a yellow oil (0.95 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969713B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-5ea9392bbf1b4a8a95dc14d7800a3be4 |
| Source note | uspto-grants-2005_11 |