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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Phenylmethyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonane, hydrochloride (1:2) | HCID 18540370 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane | HCID 16036407 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217708B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-a919a63f10f64692b0e270702648bfda |
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| Source note | uspto-grants-2007_05 |
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