HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782230Generated: October 29, 2026
Hydrochloric Acid → [5-Bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methanol
https://huagongshe.com/reaction/1782230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | methyl 5-bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carboxylate | HCID 66924623 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [5-Bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methanol | HCID 66924670 | 108.9% |
Reaction Steps
A solution (80 mL) of methyl 5-bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carboxylate (7.1 g) in tetrahydrofuran was cooled to −78° C., a 1.5 mol/L solution (42 mL) of diisobutylaluminum hydride in toluene was added dropwise over 30 min and the mixture was further stirred at −78° C. for 1 hr. 1 mol/L hydrochloric acid (20 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound as a brown oil (yield 7.1 g, about 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07498337B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-7ce408ff2a7a4fad8ca77311f2254f40 |
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| Source note | uspto-grants-2009_03 |
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