Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012403Generated: October 31, 2026

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

https://huagongshe.com/reaction/1012403

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 numberUS07977488B2
Source datasetuspto-grants-2011_07
ORD IDord-89d91a5535ae4eda91311bf853becc8e
Source noteuspto-grants-2011_07