HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(Ethylthio)benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(Ethylsulfanyl)benzoic acid | HCID 425758 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Ethylthio)benzoyl chloride | HCID 14853175 | — |
Reaction Steps
Oxalyl chloride (113 μL, 1.3 mmol) was added slowly to a stirring suspension of 2-(ethylthio)benzoic acid (1-A) (182 mg, 1.0 mmol) and 3 μL DMF in methylene chloride (2 mL). After stirring for 3.5 h at room temperature, the mixture was concentrated in vacuo to give 2-(ethylthio)benzoyl chloride (1-B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178546B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-2ab74a17a2af4612954f5b2c849d1b19 |
| Source note | uspto-grants-2012_05 |