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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808984Generated: November 1, 2026

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → tert-Butyl 3-ethylideneazetidine-1-carboxylate

https://huagongshe.com/reaction/1808984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl 3-ethylideneazetidine-1-carboxylateHCID 5218084149%

Reaction Steps

Potassium tert-butoxide (1.672 g, 14.9 mmol) and ethyltriphenylphosphonium bromide (5.538 g, 14.9 mmol) were stirred in ether (30 mL) at ambient for 1 h. 1,1-Dimethylethyl 3-oxoazetidine-1-carboxylate (954 mg, 6.0 mmol), prepared using procedures similar to those described in Example 3, was added and the mixture was 35° C. for 4.5 h. Mixture was filtered through celite and the solid was washed with ether. The filtrate was washed with water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Column chromatography (silica gel, 20% ether in hexanes) gave 1,1-dimethylethyl 3-ethylideneazetidine-1-carboxylate (506 mg, 2.76 mmol, 49% yield): 1H NMR (400 MHz, CDCl3): 5.37-5.28 (m, 1H), 4.47-4.39 (m, 4H), 1.56-1.51 (m, 3H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362002B2
Source datasetuspto-grants-2013_01
ORD IDord-f0310cd961854d28a4a25136655fc567
Source noteuspto-grants-2013_01