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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium sulfate decahydrateHCID 62649—
ReactantHydrideHCID 166653—
ReactantPotassium FluorideHCID 522689—
ReactantLithiumHCID 3028194—
ReactantEthyl5-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-[(methylsulfonyl)amino]benzoateHCID 57762930—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-(hydroxymethyl)phenyl]methanesulfonamideHCID 68714531—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566739B2
Source datasetuspto-grants-2009_07
ORD IDord-3487f9bb3822493791449ce751f850a6
Source noteuspto-grants-2009_07