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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367776Generated: October 27, 2026

Hydrochloric Acid → 9-Methyl-3-oxa-9-azatricyclo(3.3.1.02,4)nonan-7-ol

https://huagongshe.com/reaction/1367776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178481191HCID 178481191—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product9-Methyl-3-oxa-9-azatricyclo(3.3.1.02,4)nonan-7-olHCID 27443950%

Reaction Steps

Sodium borohydride (39.0 g, 1.03 mol) was added portionwise to a stirred suspension of scopolamine (75 g, 171 mmol) in ethanol (743 mL), at 0° C. under a nitrogen atmosphere and the reaction mixture was stirred at ambient temperature for 24 h. The mixture was then acidified with 2M hydrochloric acid in diethyl ether (600 mL) and stirred for another 24 h at ambient temperature. The reaction mixture was filtered and the resulting solid was washed with diethyl ether. The dried solid was dissolved in the minimum amount of 10% aqueous potassium carbonate solution and extracted with trichloromethane (6×150 mL). The combined organic extracts were dried (magnesium sulfate), filtered and the solvent was removed under reduced pressure to give the title compound as crystals (13.2 g, 85.5 mmol, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893256B2
Source datasetuspto-grants-2011_02
ORD IDord-7bfb0a2860e34a79b812a3e5f69f825f
Source noteuspto-grants-2011_02