HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Allyloxycarbonylaminoacetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | N-[(allyloxy)carbonyl]glycine | HCID 11964402 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Allyloxycarbonylaminoacetyl chloride | HCID 14588174 | — |
Reaction Steps
A solution of N-(allyloxycarbonyl)glycine (described in Chem. Pharm. Bull., 48, 716 (2000); 600 mg, 3.77 mmol) in dichloromethane (15 ml) was cooled to 0° C., and N,N-dimethylformamide (0.03 ml) and oxalyl chloride (0.6 g, 4.7 mmol) were added thereto. The mixture was stirred at room temperature for 1 hour, then toluene was added thereto, and the solvent was distilled off under reduced pressure to give crude 2-(allyloxycarbonylamino)acetyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230023B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-a1399b6f79f04d07ba7510fa13d21ea7 |
| Source note | uspto-grants-2007_06 |