HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → Methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-((3-Methoxy-3-oxopropylthio)methyl)benzoic acid | HCID 43408254 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate | HCID 86705202 | 91.7% |
Reaction Steps
Into a 50-mL round bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-((3-methoxy-3-oxopropylthio)methyl)benzoic acid (61.6 mg, 0.24 mmol, 1.00 equiv) in dichloromethane (5 mL). This was followed by dropwise addition of oxalyl dichloride (121.76 mg, 0.96 mmol, 4.00 equiv) with stirring at room temperature. Then a few drops of N,N-dimethylformamide were added as catalyst. The resulting solution was heated to reflux for 30 min. The resulting mixture was concentrated under vacuum to yield 60 mg (crude) of methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate as yellow oil. The crude was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809339B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-ec000f5f55d64c1ba9a5ae3e713ab2b6 |
| Source note | uspto-grants-2014_08 |