HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54846Generated: October 28, 2026
Toluene → 2-Hydroxyethyl-1-(4-methylphenyl)sulfonyl-1H-indole
https://huagongshe.com/reaction/54846
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Nod-IN-1 | HCID 14783456 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Hydroxyethyl-1-(4-methylphenyl)sulfonyl-1H-indole | HCID 16203090 | 98% |
Reaction Steps
To stirred solution of Red-A1 (sodium dihydro-bis(2-methoxyethoxy)aluminate≈70% in toluene) (30 mL) in dry THF (100 mL) cooled at 5° C. and under nitrogen was added dropwise and at this temperature a solution of compound of step 1 (26,8 g, 78 mmol) in dry THF (75 mL). After stirring one hour at 5° C. and then one hour at room temperature the mixture was cooled at 10° C. and treated dropwise with 2N NaOH, to effect hydrolysis of the intermediate complex. The organic phase was separated and the solvent in vacuo evaporated. The residue was solved in ethyl ether, the solution washed with water, dried over MgSO4 and evaporated to give the required alcohol (23.3 g, 98%) as a yellow oil; IR (film) 3500, 1597 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05622983 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-3ea63432e65e4a2ba31124427b761214 |
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| Source note | uspto-grants-1997_04 |
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