HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 19434018, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Amino-1-butanol | HCID 25868 | — |
| Reactant | 2-(3-Thienyl)-1,3-dioxolane | HCID 315630 | — |
| Reactant | 3-(1,3-dioxolan-2-yl)thiophene-2-sulfonyl Chloride | HCID 10538915 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 19434018 | HCID 19434018 | 62% |
Reaction Steps
A solution of 3-(1,3-dioxolan-2-yl)-thiophene-2-sulfonyl chloride, prepared from thiophene-3-carboxaldehyde ethylene acetal (20.0 g, 128 mmol) as described in Example 6, Step A, was combined with 4-amino-1-butanol (17.1 g, 192 mmol) and triethylamine (15 g, 148 mmol). The reaction was stirred for 1 h, a saturated aqueous solution of sodium bicarbonate (200 mL) was added and this mixture was stirred for 1 h. The organic layer was separated, dried (MgSO4), and evaporated to a residue which was purified by column chromatography (silica, 50% ethyl acetate/hexane to ethyl acetate, gradient) to give an oil (26.45 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538966 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-d9df0f99478a4f689971c89dd8c8370d |
| Source note | uspto-grants-1996_07 |