Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078436Generated: October 30, 2026

Water → 3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane

https://huagongshe.com/reaction/2078436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11268889HCID 11268889—
SolventTolueneHCID 1140—
Product3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonaneHCID 16036407—

Reaction Conditions

Temperature95 °C

Reaction Steps

Water (11.2 mL) and concentrated sulfuric acid (24.5 mL) were added to 5-benzyl-3,7-dihydroxy-1-phenylsulfonyl-1,5-diazacyclooctane (2.92 g, 7.76 mmol; see step (ii) above). The reaction mixture was heated for 24 hours at 95° C. The temperature was adjusted to 60° C., and toluene (40 mL) was added. Sodium hydroxide solution was then added (150 mL of 5 M), causing the internal temperature to rise to 85° C. The pH of the reaction mixture was then checked, and was found to be 2. A few pellets of solid sodium hydroxide were then added. The pH was measured again, and was found to be 13. The layers were separated, and the aqueous phase extracted with toluene (50 mL). The organic phases were combined, dried (MgSO4), filtered and concentrated in vacuo to provide 3-benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane as an orange-brown oil. This can be converted to the title compound (dihydrochloride salt) by reaction with hydrochloric acid under standard conditions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928225B2
Source datasetuspto-grants-2011_04
ORD IDord-ebc840ab2fdc48c1a96981fffc390c62
Source noteuspto-grants-2011_04