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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47340Generated: October 24, 2026

Ammonium Chloride → Tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate

https://huagongshe.com/en/reaction/47340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 1,1-dichloro-2-oxo-7-azaspiro[3.5]nonane-7-carboxylateHCID 9857764—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
ProductTert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylateHCID 1119579880.2%

Reaction Steps

106.1 g zinc dust was added to a mixture of 62.5 g tert-butyl 1,1-dichloro-2-oxo-7-azaspiro[3.5]nonane-7-carboxylate and 500 ml saturated ammonium chloride in methanol. The mixture was stirred for 1 hr and 20 min at room temperature and filtered through Celite. The filtrate was evaporated, 1 N hydrochloric acid/ethyl acetate was added thereto, and the organic layer was recovered. The extract was washed with water, saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated, and the resulting residue was subjected to silica gel column chromatography to give 38.9 g of tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699870B2
Source datasetuspto-grants-2004_03
ORD IDord-97e74cb0144947d491a5546620c3a145
Source noteuspto-grants-2004_03