Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352393Generated: October 30, 2026

1-(4-Methoxybenzene-1-sulfonyl)proline → 1-[(4-Methoxyphenyl)sulfonyl]-2-pyrrolidinemethanol

https://huagongshe.com/reaction/352393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Methoxybenzene-1-sulfonyl)prolineHCID 2882267—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-[(4-Methoxyphenyl)sulfonyl]-2-pyrrolidinemethanolHCID 5237916—

Reaction Steps

Part B: To a solution of 4.00 g (14 mmol) of 1-[(4-methoxyphenyl)sulfonyl]-2-carboxypyrrolidine from part A in 50 mL of anhydrous tetrahydrofuran at 0 C under a nitrogen atmosphere, was slowly added over 15 minutes, 20 mL (20 mmol) of a 1M solution of lithium aluminum hydride in diethyl ether. After stirring at room temperature for 2 hours, the solution was cooled in an ice bath, and quenched by the slow sequential addition of 0.8 mL of water, 0.8 mL of 10% sodium hydroxide and 2.4 mL of water. The resulting suspension was filtered through celite and the celite washed with ethyl acetate. The combined organic filtrates were stripped, the residue disolved in ethyl acetate, which was washed with 5% KHSO4, saturated sodium bicarbonate, brine, dried with sodium sulfate, filtered and stripped to afford 3.66 g of crude material. This was chromatographed on 200 g of silica gel using 40%-75% ethyl acetate/hexane to yield pure 1-[(4-methoxyphenyl)sulfonyl]-2-(hydroxymethyl)pyrrolidine, m/e=278 (M+Li).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747027B1
Source datasetuspto-grants-2004_06
ORD IDord-01b5c29e8dfe497eaff52a35bc7eef07
Source noteuspto-grants-2004_06