HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 19434098, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(3-Thienyl)-1,3-dioxolane | HCID 315630 | — |
| Reactant | 3-(1,3-dioxolan-2-yl)thiophene-2-sulfonyl Chloride | HCID 10538915 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19434098 | HCID 19434098 | 75% |
Reaction Steps
A solution of 3-(1,3-dioxolan-2-yl)-thiophene-2-sulfonyl chloride (11.16 g), prepared from thiophene-3-carboxaldehyde ethylene acetal as described in Example 6, Step A, in THF (100 mL) at 0° C. was combined with p-anisidine (7.87 g, 63.9 mmol) and triethylamine (4.04 g, 40 mmol). After stirring for 4 hr at ambient temperature, the mixture was evaporated to a residue which was extracted with ethyl acetate (2×150 mL). The combined extracts were dried (MgSO4) and evaporated to a residue which was purified by column chromatography (silica, 40% ethyl acetate/hexane) to give an oil (10.21 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538966 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-985edd1b453342fe82587fc02784107b |
| Source note | uspto-grants-1996_07 |