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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877697Generated: October 28, 2026

4-Toluenesulfonyl chloride → (3S,4R)-benzyl 3-ethyl-4-(tosyloxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/877697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant(3S,4R)-benzyl 3-ethyl-4-hydroxypyrrolidine-1-carboxylateHCID 46938936—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(3S,4R)-benzyl 3-ethyl-4-(tosyloxy)pyrrolidine-1-carboxylateHCID 8670789394%

Reaction Steps

(3S,4R)-benzyl 3-ethyl-4-hydroxypyrrolidine-1-carboxylate (18.9 g, 76 mmol), 4-methylbenzene-1-sulfonyl chloride (21.68 g, 114 mmol) were dissolved in DCM (100 mL) and cooled in an ice bath. Added N,N-dimethylpyridin-4-amine (1.852 g, 15.16 mmol) and triethylamine (11.51 g, 114 mmol) and let the reaction mixture warm to RT overnight. The suspension was passed over a silica column and eluted with Heptanes/EA (9:1 to 4:1 mixtures) to give (3S,4R)-benzyl 3-ethyl-4-(tosyloxy)pyrrolidine-1-carboxylate (28.7 g, 71.1 mmol, 94% yield). LCMS:M+1=404, t=3.07 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987268B2
Source datasetuspto-grants-2015_03
ORD IDord-dceec6b6e5984d0ba67e142a490a0710
Source noteuspto-grants-2015_03