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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912723Generated: November 3, 2026

4-Nitrobenzoic Acid → cis-2-(Tert-butoxycarbonyl)amino-1-(4-nitrobenzoyloxy)cyclopentane

https://huagongshe.com/reaction/1912723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoic AcidHCID 6108—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(1R,2R)-trans-N-Boc-2-AminocyclopentanolHCID 45091953—
SolventTetrahydrofuranHCID 8028—
Productcis-2-(Tert-butoxycarbonyl)amino-1-(4-nitrobenzoyloxy)cyclopentaneHCID 6913344970.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609644B2
Source datasetuspto-grants-2013_12
ORD IDord-3a2be80130c247af856ed778220502ee
Source noteuspto-grants-2013_12