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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260923Generated: November 1, 2026

Triethylamine → rel-1,1-Dimethylethyl (3R,4S)-3-amino-4-(3,4-dichlorophenyl)-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/1260923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactantrel-1-(1,1-Dimethylethyl) (3R,4S)-4-(3,4-dichlorophenyl)-1,3-pyrrolidinedicarboxylateHCID 51441167—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Productrel-1,1-Dimethylethyl (3R,4S)-3-amino-4-(3,4-dichlorophenyl)-1-pyrrolidinecarboxylateHCID 67232421100.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of the compound (14.4 g) obtained in step 5 in toluene (120 mL) were added DPPA (16.5 g) and triethylamine (8.36 mL) at room temperature, and the mixture was stirred at 100° C. for 2 hr. The reaction mixture was cooled, 8N aqueous sodium hydroxide solution (50 mL) was added, and the mixture was stirred at room temperature for 14 hr. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution and brine and dried, and the solvent was evaporated under reduced pressure to give crude tert-butyl (3R*,4S*)-3-amino-4-(3,4-dichlorophenyl)pyrrolidine-1-carboxylate (13.3 g, 100%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470816B2
Source datasetuspto-grants-2013_06
ORD IDord-a87075bbe20f4a5b8da308e9febcfbfc
Source noteuspto-grants-2013_06