HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035656Generated: October 29, 2026
3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → tert-Butyl 3-methylideneazetidine-1-carboxylate
https://huagongshe.com/reaction/2035656
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Oxo-azetidine-1-carboxylic acid tert-butyl ester | HCID 1519404 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-Butyl 3-methylideneazetidine-1-carboxylate | HCID 55269097 | 78.7% |
Reaction Steps
To a 0° C. mixture of KOtBu (5.90 g, 52.6 mmol) in 95 mL ether was added methyltriphenylphosphonium bromide (18.8 g, 52.6 mmol). The reaction mixture was warmed to ambient temperature and stirred 1.5 hours. A solution of tert-butyl 3-oxoazetidine-1-carboxylate (4.50 g, 26.3 mmol) in 10 mL ether was added. The reaction mixture was heated to reflux for 2 hours, then cooled to ambient temperature. Solids were removed by vacuum filtration through compressed Celite and rinsed with ether, and the filtrate was concentrated. The resulting residue was suspended in 1:1 hexanes:ethyl acetate, and the solids were removed by vacuum filtration through GF/F paper and rinsed with 1:1 hexanes:ethyl acetate. The filtrate was concentrated, and the resulting oil was purified on silica gel (5-20% ethyl acetate in hexanes gradient) to give the desired product (3.50 g, 78.7% yield) as a clear colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575145B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7daff68699bc4d6cb690ecc9cae1999a |
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| Source note | uspto-grants-2013_11 |
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