HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3-(4-Benzyloxyphenyl)-2-ethylsulfanyl propanoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 3-(4-benzyloxyphenyl)-2-chloropropanoate | HCID 10780869 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(4-Benzyloxyphenyl)-2-ethylsulfanyl propanoic acid methyl ester | HCID 54105132 | 86.7% |
Reaction Steps
Potassium hydroxide (0.092 g; 1.64 mmole) was dissolved in methanol. Ethanethiol (0.133 g; 2.14 mmole) and 3-(4-benzyloxyphenyl)-2-chloropropanoic acid methyl ester (0.5 g; 1.64 mmole) were added. The reaction mixture was stirred at room temperature over night. Diethyl ether (15 ml) was added. The mixture was filtered and evaporated. The residue was purified by adding active charcoal in methanol. The mixture was stirred for 15 minutes and the active charcoal was filtered off. Evaporation of the solvent gave 0.47 g (86.7% yield) of 3-(4-benzyloxyphenyl)-2-ethylsulfanyl propanoic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06630600B1 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-1073b56c4a234ce49c366e5a32311bb0 |
| Source note | uspto-grants-2003_10 |