Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351127Generated: October 27, 2026

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

https://huagongshe.com/reaction/1351127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-(Phenylmethyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonane, hydrochloride (1:2)HCID 18540370—
SolventTolueneHCID 1140—
Product3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonaneHCID 16036407—

Reaction Conditions

Temperature60 °C

Reaction Steps

All volumes and equivalents are measured with respect to the amount of 3-benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane dihydrochloride (see Preparation A(vi) above) used. Toluene (420 mL, 7 vols) and aqueous sodium hydroxide solution (2 M, 420 mL, 7 vols, 4.0 eq) were added to 3-benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane dihydrochloride (60.07 g, 206.03 mmole, 1.0 eq., see Preparation A(vi) above). The mixture was stirred under nitrogen, heated to 60° C. and held at this temperature for 30 minutes by which time two clear layers had formed. The lower, aqueous layer was removed, and the toluene solution of sub-title compound (free base) was azeodried at atmospheric pressure (total volume of solvent removed=430 mL; total volume of toluene added=430 mL), then concentrated to a volume of 240 mL (4 vols). Karl Fischer analysis at this stage showed 0.06% water in the solution. The dried solution of sub-title compound (theoretically 44.98 g, 206.03 mmole, 1.0 eq) was used as such in a subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217708B2
Source datasetuspto-grants-2007_05
ORD IDord-a919a63f10f64692b0e270702648bfda
Source noteuspto-grants-2007_05