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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260941Generated: October 31, 2026

Triethylamine → tert-butyl (3S,4R)-3-amino-4-(3,4-dichlorophenyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1260941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant(3S,4R)-1-(tert-butoxycarbonyl)-4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylic acidHCID 51441165—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Producttert-butyl (3S,4R)-3-amino-4-(3,4-dichlorophenyl)pyrrolidine-1-carboxylateHCID 5835610296%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of the compound (1.2 g) obtained in step 4 in toluene (9 mL) were added DPPA (1.06 mL) and triethylamine (0.68 mL) at room temperature, and the mixture was stirred at 100° C. for 1 hr. The reaction mixture was cooled, 8N aqueous sodium hydroxide solution (4.2 mL) was added, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with water and brine and dried, and the solvent was evaporated under reduced pressure to give tert-butyl (3S,4R)-3-amino-4-(3,4-dichlorophenyl)pyrrolidine-1-carboxylate (1.06 g, 96%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470816B2
Source datasetuspto-grants-2013_06
ORD IDord-998f8cd05a464e0585f1dc6a2ec006c5
Source noteuspto-grants-2013_06