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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582032Generated: October 30, 2026

Hydrochloric Acid → 8-(Propan-2-yl)-8-azabicyclo[3.2.1]octan-3-one

https://huagongshe.com/reaction/582032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
ReactantAcetonedicarboxylic acidHCID 68328—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
ReactantSodium AcetateHCID 517045—
CatalystHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product8-(Propan-2-yl)-8-azabicyclo[3.2.1]octan-3-oneHCID 10300927.6%

Reaction Steps

2M Hydrochloric acid (8 drops) was added to a stirred solution of 2,5-dimethoxytetrahydrofuran (16.5 g) in water (70 ml). After 15 minutes a mixture of diisopropylamine (7.38 g) and 2M hydrochloric acid (40 ml) was added to the reaction followed by acetonedicarboxylic acid (18.25 g) and sodium acetate (10.0 g) in water (100 ml). After 3 days 1,3-acetonedicarboxylic acid (6.0 g) and sodium acetate (3.0 g) were added. After a further 6 days the mixture was basified to pH8 and extracted with ethyl acetate. The extracts were dried (MgSO4) and evaporated under reduced pressure. The aqueous fraction was then extracted with chloroform and the extracts dried (MgSO4) and evaporated under reduced pressure. Distillation of the combined extracts (95-115° C.; 18 mmHg) gave 8-isopropyl-8-azabicyclo[3.2.1]octan-3-one (3.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922732
Source datasetuspto-grants-1999_07
ORD IDord-82ecd606e11f4d628e4c9afecfb1f8e8
Source noteuspto-grants-1999_07