HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 5-Nitrothiophene-3-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-nitrothiophene-3-carboxylic acid | HCID 2777267 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Nitrothiophene-3-carbonyl chloride | HCID 13275558 | — |
Reaction Steps
To a suspension of 5-nitro-thiophene-3-carboxylic acid (5.0 g, 29 mmol) in dichloromethane (60 ml) was added oxalyl chloride (2.93 ml, 35 mmol) at room temperature. The mixture was stirred for 30 minutes at room temperature then for 30 minutes at 50° C. The solvent was evaporated and the residue suspended in tetrahydrofuran (30 ml). The solution was used without purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08252936B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-195c8100da24441c91ddbea8e4b4529a |
| Source note | uspto-grants-2012_08 |