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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555387Generated: October 30, 2026

Benzyl 4-Hydroxybenzoate → 952589-12-7

https://huagongshe.com/reaction/555387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-HydroxybenzoateHCID 7180—
ReactantTriphenylphosphineHCID 11776—
Reactant1-Boc-3-pyrrolidinolHCID 4416939—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
Product952589-12-7HCID 2270980769.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-hydroxy-pyrrolidine-1-carboxylic acid t-butyl ester (3 g, 16.02 mmol) in dry THF (75 mL) was added triphenyl phosphine (4.62 g, 17.62 mmol) and 4-hydroxy-benzoic acid benzyl ester (4.02 g, 17.62 mmol). The reaction mixture was cooled to 0° C. and DEAD (2.78 mL, 17.62 mmol) was added dropwise over a period of 30 min. The reaction was gradually brought to room temperature and stirring continued for 16 hrs. The solvent was removed under vacuum and the residue purified by column chromatography (Flash 40) using a gradient of starting from EtOAc-heptane 1:20 to 1:5. Desired fractions were collected and the solvent evaporated in vacuo. The residue was dissolved in EtOH (80 mL) and 10% Pd/C (0.5 g) was added and the mixture was hydrogenated for 16 hrs. The mixture was filtered and the volatiles were evaporated in vacuo affording 3.4 g (69%) of 3-(4-carboxy-phenoxy)-pyrrolidine-1-carboxylic acid t-butyl ester as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053447B2
Source datasetuspto-grants-2011_11
ORD IDord-dee2548d347f4a3abf9490eb41fb0846
Source noteuspto-grants-2011_11