Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-Azabicyclo[3.3.1]nonan-4-ol | HCID 18986107 | — |
| Product | HCID 66679631 | HCID 66679631 | 87% |
Reaction Steps
To acetic anhydride (150 ml) (4SR,5RS)-(1-aza-bicyclo[3.3.1]nonan-4-ol (21.34 g, 151 mmol) is added portionwise under cooling. The reaction mixture is heated to 120° C. for 2.5 h, is evaporated and extracted with THF/sat. K2CO3 soln. The aq. layer is reextracted with THF. The combined organic layers are washed with brine, dried over Na2SO4, filtered and evaporated. The crude product is purified by bulb-to-bulb distillation (HV, 90° C.) to give 24.07 g (87%) of (4SR,5RS)-acetic acid 1-aza-bicyclo[3.3.1]non-4-yl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713976B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-424f276b4ca247268ecfdfec9494c5c6 |
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| Source note | uspto-grants-2010_05 |
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