HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489821Generated: October 30, 2026
Sulfur Dioxide → 3-(2-Hydroxypropyl)thiophene-2-sulfonamide
https://huagongshe.com/reaction/1489821
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(Thiophen-3-yl)propan-2-ol | HCID 22901911 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-Hydroxypropyl)thiophene-2-sulfonamide | HCID 22901969 | 42% |
Reaction Steps
To a solution of 3-(2-hydroxypropyl)thiophene (2.95 g, 20.77 mmol) i THF (25 mL) at -78° C. was added n-butyllithium (18.3 mL of a 2.5M solution, 45.69 mmol). This mixture was stirred at -78° C. for 1 hr and sulfur dioxide was added until the solution maintained a pH of 3. The reaction mixture was warmed to room temperature, stirred for 30 min, and evaporated to a residue which was dissolved in water (25 mL). Sodium acetate (5.1 g, 62.31 mmol) and hydroxylamine-O-sulfonic acid (7.0 g, 62.31 mmol) were added, the mixture stirred at room temperature for 18 hr, and the pH was adjusted to 8 with sodium bicarbonate. This solution was extracted with ethyl acetate (2×200 mL), the extracts were dried (MgSO4) and evaporated to a residue which was purified by column chromatography (silica, 50% hexane/ethyl acetate) to give 1.9 g (42%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05679670 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-6e558ce9c7fa4c8fa411f225398b80e8 |
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| Source note | uspto-grants-1997_10 |
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