HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 12905148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 12336141 | HCID 12336141 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 12905148 | HCID 12905148 | — |
Reaction Steps
Oxalyl chloride (5.3 g) was added to a solution of 2,3-diacetoxybenzamide (4.0 g) in 1,2-dichloroethane (40 ml) with stirring under cooling. The mixture was gradually heated to a reflux temperature and allowed to react under reflux for 10 hours. Then, the solvent and excess oxalyl chloride were distilled off under reduced pressure to give 2,3-diacetoxybenzoyl isocyanate, which was dissolved in anhydrous dichloromethane (40 ml) for the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229348 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-2c7180cf420242daa7aa9fc3eb789356 |
| Source note | uspto-grants-1980_10 |