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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate | HCID 67043967 | — |
| Reactant | Hydride toluene | HCID 86595848 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | {1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanol | HCID 67044165 | 77.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855225B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-15f54747040349eea6a878198eab5a52 |
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| Source note | uspto-grants-2010_12 |
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