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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522877Generated: October 31, 2026

4-Chlorophenol → Tert-butyl 3-(1-(4-chlorophenoxy)ethyl)-azetidine-1-carboxylate

https://huagongshe.com/reaction/522877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantTert-butyl 3-(1-hydroxyethyl)azetidine-1-carboxylateHCID 58348207—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-(1-(4-chlorophenoxy)ethyl)-azetidine-1-carboxylateHCID 8668524244.2%

Reaction Steps

To a flask charged with tert-butyl 3-(1-hydroxyethyl)azetidine-1-carboxylate (212 mg, 1.053 mmol) was added THF (6.3 mL), resin bound PPh3 (527 mg, 1.580 mmol), p-chlorophenol (104 μL, 1.053 mmol) and DEAD (250 μL, 1.580 mmol). The reaction mixture was stirred overnight at RT. The reaction mixture was filtered through cotton and dried under reduced pressure, then purified with flash chromatography ramping CH2Cl2:MeOH:NH4OH (90:10:1) in CH2Cl2 from 0% to 100% to afford tert-butyl 3-(1-(4-chlorophenoxy)ethyl)-azetidine-1-carboxylate (145 mg, 44%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-c31e993c8b884d888ca467cb33b4e20b
Source noteuspto-grants-2016_05