HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230592Generated: October 26, 2026
Sodium sulfate decahydrate → N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-(hydroxymethyl)phenyl]methanesulfonamide
https://huagongshe.com/reaction/230592
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Hydride | HCID 166653 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Ethyl5-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-[(methylsulfonyl)amino]benzoate | HCID 57762930 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-(hydroxymethyl)phenyl]methanesulfonamide | HCID 68714531 | — |
Reaction Steps
To a mixture of lithium alminium hydride (1.6 g, 43 mmol) in tetrahydrofuran (THF) (50 ml) was added a solution of ethyl 5-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-[(methylsulfonyl)amino]benzoate (4.2 g, 11 mmol) in tetrahydrofuran (THF) (100 ml) at 0° C. After being stirred for 3 hours at 0° C., potassium fluoride and sodium sulfate decahydrate were added. After being stirred for 5 hours, the reaction mixture was filtered and the filtrate was evaporated under reduced pressure to give 3.6 (97% yield) of the title compound as slightly yellow oil. MS (ESI) m/z 391 [M+H]+, 389 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566739B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-3487f9bb3822493791449ce751f850a6 |
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| Source note | uspto-grants-2009_07 |
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