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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376009Generated: October 26, 2026

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

https://huagongshe.com/reaction/1376009

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 step (iv) above) used. Toluene (420 mL, 7 vols) and aqueous sodium hydroxide solution (2M, 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 step (iv) 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 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 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 numberUS07169921B2
Source datasetuspto-grants-2007_01
ORD IDord-7790cf68d61f45708249b322652265c5
Source noteuspto-grants-2007_01