HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943595Generated: November 1, 2026
Trichloroacetyl chloride → tert-Butyl 5,5-dichloro-6-oxo-2-azaspiro[3.3]heptane-2-carboxylate
https://huagongshe.com/reaction/1943595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | tert-Butyl 3-methylideneazetidine-1-carboxylate | HCID 55269097 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-Butyl 5,5-dichloro-6-oxo-2-azaspiro[3.3]heptane-2-carboxylate | HCID 69669942 | — |
Reaction Steps
Under an inert atmosphere, 7.728 g (118.19 mmoles) of zinc in nanopowder form are suspended in 100 ml of diethyl ether. 5.00 g (29.55 mmoles) of tert-butyl 3-methylene-azetidine-1-carboxylate (WO 2008124085) are added, then the medium is cooled to 10° C. A solution of 6.60 ml (59.09 mmoles) of trichloroacetyl chloride in ml of 1,2-dimethoxyethane is added drop by drop while maintaining the temperature of the reaction medium between 26 and 30° C. After stirring for 14 hrs at ambient temperature, the medium is filtered over celite, the celite is copiously rinsed with diethyl ether and the filtrate is partially concentrated under reduced pressure. The crude reaction product thus obtained is used as such in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394787B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-ade1e48e085e4c8d910f142994fe43b5 |
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| Source note | uspto-grants-2013_03 |
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