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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070388Generated: November 1, 2026

Hydrochloric Acid → [5-Bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methanol

https://huagongshe.com/reaction/2070388

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 numberUS08299261B2
Source datasetuspto-grants-2012_10
ORD IDord-b12d8f9042114371b36c65877f964c4b
Source noteuspto-grants-2012_10