HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Methyl 5-(chloromethyl)thiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methyl 5-(hydroxymethyl)thiophene-3-carboxylate | HCID 12926498 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-(chloromethyl)thiophene-3-carboxylate | HCID 12926494 | — |
Reaction Steps
4.86 g of methyl 5-(hydroxymethyl)thiophene-3-carboxylate was dissolved in 50.0 mL of dichloromethane, and 4.12 mL of thionyl chloride was added thereto under ice-cooling, followed by stirring at room temperature for 15 hours. The reaction liquid was concentrated under reduced pressure, and to the obtained residue was added ethyl acetate, and then washed with an aqueous saturated sodium hydrogen carbonate solution and saturated brine. It was dried over anhydrous magnesium sulfate, and then the solvent was evaporated to obtain 4.90 g of methyl 5-(chloromethyl)thiophene-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973078B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-54a1ca223ad44f0b89855ad551186b9b |
| Source note | uspto-grants-2011_07 |