HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1-(2-(tert-butyl)phenyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2,5-Pyrrolidinedione, 1-[2-(1,1-dimethylethyl)phenyl]- | HCID 10799525 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-(tert-butyl)phenyl)pyrrolidine | HCID 10845838 | 80% |
Reaction Steps
To a solution of 1-(2-tert-butylphenyl)pyrrolidine-2,5-dione (500 mg, 2.16 mmol) in THF (10 mL) was added BH3 in toluene (350 mg, 1.72 mmol) dropwise and the reaction mixture was heated to reflux overnight. The reaction was cooled to room temperature and quenched with methanol (until the evolution of H2 ceased). The solvent was evaporated to obtain 1-(2-tert-butylphenyl)pyrrolidine (350 mg, 80%) as an oil. 1H NMR (400 MHz, CDCl3) δ 7.30 (s, 1H), 7.28 (s, 1H), 7.15 (d, J=0.9 Hz, 1H), 7.07-7.01 (m, 1H), 2.90 (s, 4H), 1.88-1.78 (m, 4H), 1.35 (s, 9H). LC/MS: m/z 204.1 (M+H)+ at 0.88 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802700B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-07124868889549ddb913837c7d7b99c3 |
| Source note | uspto-grants-2014_08 |