HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 4-Hydroxybenzoate → 2-benzyl 1-tert-butyl (2S,4S)-4-{4-[(benzyloxy)carbonyl]phenoxy}pyrrolidine-1,2-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 4-Hydroxybenzoate | HCID 7180 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | Boc-hyp-obzl | HCID 11902907 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-benzyl 1-tert-butyl (2S,4S)-4-{4-[(benzyloxy)carbonyl]phenoxy}pyrrolidine-1,2-dicarboxylate | HCID 90291098 | 29.2% |
Reaction Steps
To a solution of 2-benzyl 1-tert-butyl (2S,4R)-4-hydroxypyrrolidine-1,2-dicarboxylate (565 mg) in tetrahydrofuran (10.0 mL) were added benzyl 4-hydroxybenzoate (405 mg) and 1,1′-(azodicarbonyl)dipiperidine (555 mg), and then tri-n-butyl phosphine (0.540 mL) was added thereto under ice-cooling, followed by stirring at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and then the residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 2-benzyl 1-tert-butyl (2S,4S)-4-{4-[(benzyloxy)carbonyl]phenoxy}pyrrolidine-1,2-dicarboxylate (273 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199927B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-cd24e1c71e414ea1989978de95e7f3f7 |
| Source note | uspto-grants-2015_12 |