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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553432Generated: October 27, 2026

Acetic Anhydride → HCID 66679631, compound

https://huagongshe.com/reaction/553432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-Azabicyclo[3.3.1]nonan-4-olHCID 18986107—
ProductHCID 66679631HCID 6667963187%

Reaction Conditions

Temperature120 °C

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 reextiacted 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048885B2
Source datasetuspto-grants-2011_11
ORD IDord-bd5be6a79c5d4cd593e3cb56e3e13ac1
Source noteuspto-grants-2011_11