HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Methyl 4-[(2-methoxy-2-oxoethyl)sulfanyl]butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | Butanoic acid, 4-chloro-, methyl ester | HCID 76612 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-[(2-methoxy-2-oxoethyl)sulfanyl]butanoate | HCID 18379236 | 105.5% |
Reaction Steps
Sodium (3.5 g, 0.15 mol) was added to methanol (150 mL) carefully. After cooling to room temperature, methyl 2-mercaptoacetate (15.6 g, 0.13 mol) was added. The mixture was stirred for 30 mins at room temperature and a little of NaI and methyl 4-chlorobutanoate 20.0 g, 0.15 mol) were added. The reaction mixture was refluxed over night. After cooling to room temperature, the solvent was removed under reduced pressure, then the residue was dissolved in CH2Cl2 (100 mL). The solution was washed with H2O (30 mL), brine (30 mL), and dried with Na2SO4. After removing the solvent, 28.3 g of the crude product was obtained (Yield: 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372875B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-92fddd1e7eb644278ea68af7f2899561 |
| Source note | uspto-grants-2013_02 |