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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant1,2-DimethoxyethaneHCID 8071—
Reactanttert-Butyl 3-methylideneazetidine-1-carboxylateHCID 55269097—
CatalystZincHCID 23994—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl 5,5-dichloro-6-oxo-2-azaspiro[3.3]heptane-2-carboxylateHCID 69669942—

Reaction Conditions

Temperature10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394787B2
Source datasetuspto-grants-2013_03
ORD IDord-ade1e48e085e4c8d910f142994fe43b5
Source noteuspto-grants-2013_03