HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 2-methoxy-5-methylthiobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178489964 | HCID 178489964 | — |
| Solvent | Methylenechloride Hexane | HCID 21226440 | — |
| Product | Methyl 2-methoxy-5-methylthiobenzoate | HCID 53727199 | — |
Reaction Steps
Combine 2-methoxy-5-methylthiobenzoic acid (6.82 g, 34.4 mmol) and methanol (65 mL). Cool in an ice bath. Add slowly dropwise thionyl chloride (2.8 mL, 38 mmol). Warm to ambient temperature. After 18 hours, evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 25% hexane/dichloromethane to give methyl 2-methoxy-5-methylthiobenzoate: Rf=0.06 (silica gel, 65% hexane/dichloromethane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194406B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-6b0b09a066dd4ea0b855f9b5cd278faf |
| Source note | uspto-grants-2001_02 |