HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (2S)-2-(phenoxymethyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (S)-tert-Butyl 2-(phenoxymethyl)pyrrolidine-1-carboxylate | HCID 10636271 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S)-2-(phenoxymethyl)pyrrolidine | HCID 9855629 | 79.8% |
Reaction Steps
To a solution of (S)-(+)-N-Boc-2-phenoxymethylpyrrolidine (0.81 g. 2.9 mmol) in 5 mL of CH2Cl2 in 0° C. was added 5 mL of TFA dropwise over 1 hour. The solution was warmed to room temperature and stirred for 1.5 hours. The reaction mixture was slowly poured into 30 mL of 10% NaOH and extracted thrice with 20 mL CH2Cl2. The organic layer was then dried over Na2SO4, filtered and concentrated under reduced pressure to give a light yellow oil (0.41 g, 79%). ES (+) MS m/e=178 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403792B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-39b6952065504f61b163ddc4571c2dcb |
| Source note | uspto-grants-2002_06 |