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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047440Generated: October 31, 2026

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

https://huagongshe.com/reaction/2047440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-(Tert-butoxycarbonyl)-4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylic acidHCID 16244062—
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) was 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 solution 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 extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution and saturated brine, dried, and concentrated under reduced pressure to give tert-butyl (3R*,4S*)-3-amino-4-(3,4-dichlorophenyl)pyrrolidine-1-carboxylate (13.3 g, 100%) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592454B2
Source datasetuspto-grants-2013_11
ORD IDord-ef17aca1ac414e8d842e96b41c7b167f
Source noteuspto-grants-2013_11