HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzoic Acid → cis-2-(Tert-butoxycarbonyl)amino-1-(4-nitrobenzoyloxy)cyclopentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzoic Acid | HCID 6108 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (1R,2R)-trans-N-Boc-2-Aminocyclopentanol | HCID 45091953 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | cis-2-(Tert-butoxycarbonyl)amino-1-(4-nitrobenzoyloxy)cyclopentane | HCID 69133449 | 70.8% |
Reaction Steps
To a solution of trans-2-(tert-butoxycarbonyl)aminocyclopentan-1-ol (Prepn. 47, 3.00 g) triphenyl phosphine (5.90 g) and 4-nitrobenzoic acid (2.50 g) in THF (90 mL) was added, at 0° C., diisopropyl azodicarboxylate (4.50 mL). After stirring for 4 h, the solvent was evaporated and the crude product was purified by flash chromatography (SiO2, CH2Cl2:acetone 99:1) to give cis-2-(tert-butoxycarbonyl)amino-1-(4-nitrobenzoyloxy)cyclopentane (3.70 g, 70%). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 8.33 (2H, d), 8.23 (2H, d), 7.08 (1H, d), 5.25 (1H, m), 3.92 (1H, m), 1.40-2.10 (6H, m), 1.28 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609644B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-3a2be80130c247af856ed778220502ee |
| Source note | uspto-grants-2013_12 |