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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | rel-1-(1,1-Dimethylethyl) (3R,4S)-4-(3,4-dichlorophenyl)-1,3-pyrrolidinedicarboxylate | HCID 51441167 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | rel-1,1-Dimethylethyl (3R,4S)-3-amino-4-(3,4-dichlorophenyl)-1-pyrrolidinecarboxylate | HCID 67232421 | 100.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470816B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-a87075bbe20f4a5b8da308e9febcfbfc |
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| Source note | uspto-grants-2013_06 |
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