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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077101Generated: November 3, 2026

Lithium hydroxide, monohydrate → 2-Methyl-2-(tetrahydro-pyran-4-ylmethanesulfonyl)-propionic acid

https://huagongshe.com/reaction/2077101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant2-Methyl-2-(tetrahydro-pyran-4-ylmethanesulfonyl)-propionic acid ethyl esterHCID 59703934—
SolventSodium hydrogencarbonate brineHCID 129703874—
Product2-Methyl-2-(tetrahydro-pyran-4-ylmethanesulfonyl)-propionic acidHCID 59703992105.9%

Reaction Steps

To a solution of 769 mg (2.77 mmol) of 2-methyl-2-(tetrahydro-pyran-4-ylmethanesulfonyl)-propionic acid ethyl ester in THF/water (1/1, 10 mL) were added 228 mg (5.43 mmol) of lithium hydroxide monohydrate. The reaction was stirred at room temperature for 18 h. The reaction was concentrated under reduced pressure. The residue was dissolved in water (10 mL) and washed with diethyl ether (2×25 mL). The aqueous layer was cooled in an ice bath and then acidified with 1M aqueous HCl solution to pH 2. The acidic aqueous layer was extracted with ethyl acetate (2×50 mL) and with isopropanol/chloroform (3×50 mL). The combined organic extracts were dried over Na2SO4 and filtered. Concentration of the filtrate under reduced pressure afforded 734 mg of 2-methyl-2-(tetrahydro-pyran-4-ylmethanesulfonyl)-propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928123B2
Source datasetuspto-grants-2011_04
ORD IDord-0a9ce9bb8ae24df9ab251de421e2de62
Source noteuspto-grants-2011_04