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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465717Generated: October 31, 2026

tert-butyl (1R,5S)-3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate → HCID 86695584, compound

https://huagongshe.com/reaction/1465717

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (1R,5S)-3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylateHCID 688612—
ReactantLithium diisopropylamideHCID 2724682—
ReactantCarbonocyanidateHCID 21977064—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86695584HCID 8669558479.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

N-Boc-nortropinone (10 g, 44.4 mmol) was dissolved in THF (55 mL) and cooled to −78° C., LDA (2M in THF, 24.4 mL, 48.8 mmol) was added dropwise. After 1 h at −78° C., cyanoformate (4.22 mL, 53.2 mmol) was added, and the reaction mixture was warmed up to room temperature and stirred for 5 hours. After quench with saturated NH4Cl, the reaction mixture was extracted with EtOAc. The combined EtOAc layer was washed with water and brine. Dried and concentrated. The crude product was column purified with mixture of Hexane and EtOAc to give 10 g of (1S,5R)-8-tert-butyl 2-methyl 3-oxo-8-azabicyclo[3.2.1]octane-2,8-dicarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999966B2
Source datasetuspto-grants-2015_04
ORD IDord-430429739505404bae4bcadc325c75a8
Source noteuspto-grants-2015_04