HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32940Generated: October 29, 2026
Sodium Hydroxide → 2-(6-chloro-5-fluoro-1H-indol-2-yl)-1-ethylsulfanyl-propan-2-ol
https://huagongshe.com/reaction/32940
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(6-chloro-5-fluoro-1-methanesulfonyl-1H-indol-2-yl)-1-ethylsulfanyl-propan-2-ol | HCID 11588672 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(6-chloro-5-fluoro-1H-indol-2-yl)-1-ethylsulfanyl-propan-2-ol | HCID 11507523 | — |
Reaction Steps
To a solution of 2-(6-chloro-5-fluoro-1-methanesulfonyl-1H-indol-2-yl)-1-ethylsulfanyl-propan-2-ol (0.30 g, 0.82 mmol) in methanol (10 mL) was added 4M sodium hydroxide solution (0.4 mL). The reaction was allowed to proceed overnight at room temperature. Complete reaction was not achieved, so additional 1 M sodium hydroxide solution (1 mL) was added and the reaction mixture was heated to 50° C. The reaction mixture was kept at 50° C. for two hours then allowed to stir overnight at room temperature. The reaction mixture was concentrated and to the concentrate was added 1N hydrochloric acid solution and water. The mixture was extracted twice with ethyl ether. The extracts were dried over Mg2SO4, filtered, and evaporated to yield a residue. The residue was purified by column chromatography eluting with dichloromethane to yield the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07427682B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-da515cf557704a11975ab21fdc4dbd19 |
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| Source note | uspto-grants-2008_09 |
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