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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactantmethyl 5-bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carboxylateHCID 66924623—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product[5-Bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methanolHCID 66924670108.9%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498337B2
Source datasetuspto-grants-2009_03
ORD IDord-7ce408ff2a7a4fad8ca77311f2254f40
Source noteuspto-grants-2009_03