HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 5-(3,4-Dichlorobenzyl-carbamoyl)-thiophene-2-carbonyl-chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-(3,4-Dichlorobenzyl-carbamoyl)-thiophene-2-carboxylic acid | HCID 18617115 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(3,4-Dichlorobenzyl-carbamoyl)-thiophene-2-carbonyl-chloride | HCID 18617125 | — |
Reaction Steps
A stirring solution of (12(b)) (495 mg; 1.5 mmole) in dichloromethane (25 mL) was cooled in an ice bath and DMF (1 drop) and oxalyl chloride (0.175 mL; 2.0 mmole) added dropwise. The solution was stirred at ambient temperature under argon for 4 hours. The dichloromethane and excess oxalyl chloride were removed in vacuo. The residue was azeotroped uith toluene (2×15 mL) to give 5-(3,4-dichlorobenzyl-carbamoyl)-thiophene-2-carbonyl-chloride (12(c)) which was used crude in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06232338B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-c40991672c294059942cac1dbff3f3dd |
| Source note | uspto-grants-2001_05 |