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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 11268889 | HCID 11268889 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane | HCID 16036407 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928225B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-ebc840ab2fdc48c1a96981fffc390c62 |
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| Source note | uspto-grants-2011_04 |
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