HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 131720095, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | HCID 131720096 | HCID 131720096 | — |
| Product | HCID 131720095 | HCID 131720095 | — |
Reaction Steps
trans-2-(3-Methoxy-4-methylsulfoxyethoxy-5-iodophenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran (2.5 g, 4.11 mmol) was dissolved in 50 mL ethanol. To this solution was added 4-chlorothiophenol (1.19 g, 8.22 mmol) and trimethylamine (0.831 g, 8.22 mmol). The reaction mixture was refluxed for 16 hours and then the solvent was removed in vacuo. The residue was purified by column chromatography (silica, 3:1 hexane/ethyl acetate)(2.35 g, 87%). 1H NMR (CDCl3): 1.97 (m, 2H); 2.45 (m, 2H); 3.35 (t, 2H); 3.82 (s, 3H); 3.84 (s, 3H), 3.88 (s, 6H); 4.11 (t, 2H); 5.17 (m, 2H), 6.61 (s, 2H); 6.92 (s, 1H); 7.26 (d, 2H); 7.33 (d, 2H); 7.35 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294574B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-d6293e0d469742e78d236903370cd854 |
| Source note | uspto-grants-2001_09 |