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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808243Generated: October 25, 2026

3-Chlorophenol → tert-Butyl (2S)-2-[(3-chlorophenoxy)methyl]pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1808243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorophenolHCID 7933—
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(S)-(-)-N-Boc-prolinolHCID 643448—
Producttert-Butyl (2S)-2-[(3-chlorophenoxy)methyl]pyrrolidine-1-carboxylateHCID 57732115—

Reaction Steps

A solution of diisopropyl azodicarboxylate (1.4 mL, 7.1 mmol) in THF (3.5 mL, 44 mmol) was slowly added to a 0° C. solution of BOC-PRO-OL (1.0 g, 5.0 mmol), 3-chlorophenol (0.68 g, 5.2 mmol) and triphenylphosphine (1.5 g, 5.8 mmol) in THF (17 mL, 210 mmol). The reaction mixture was warmed to ambient temperature. After 3 h the reaction mixture was quenched with 1 N NaOH and extracted with methylene chloride (3×). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified on the Isco (120 g cartridge, hexanes to ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357711B2
Source datasetuspto-grants-2013_01
ORD IDord-1b69d4e09b30414ca0eb17ee395a710e
Source noteuspto-grants-2013_01