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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264626Generated: October 31, 2026

Sodium Sulfate → {1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanol

https://huagongshe.com/reaction/2264626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantSodium sulfate decahydrateHCID 62649—
Reactantethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylateHCID 67043967—
ReactantHydride tolueneHCID 86595848—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product{1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanolHCID 6704416577.2%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 1.4 g of ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate in 10 mL of THF, 7.6 mL of diisobutylalminum hydride-toluene solution was added at a temperature of −60° C. or lower, and the resulting mixture was stirred under cooling in a dry ice-acetone bath for 5 hours and under ice cooling for 2 hours. After the solution was cooled to −70° C., 5 g of sodium sulfate decahydrate and 5 mL of methanol were added, the resulting mixture was warmed to room temperature, 50 mL of ethyl acetate and anhydrous sodium sulfate were added, insoluble matter was removed by filtration, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform) to obtain 0.97 g of {1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanol as a pale violet solid. EI: 365, 367

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855225B2
Source datasetuspto-grants-2010_12
ORD IDord-15f54747040349eea6a878198eab5a52
Source noteuspto-grants-2010_12