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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237763Generated: October 30, 2026

9-(4-Benzyloxy-phenyl)-bicyclo[3.3.1]nonan-9-ol → 9-(4-Benzyloxy-phenyl)-bicyclo[3.3.1]nonane

https://huagongshe.com/reaction/237763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-(4-Benzyloxy-phenyl)-bicyclo[3.3.1]nonan-9-olHCID 67061007—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product9-(4-Benzyloxy-phenyl)-bicyclo[3.3.1]nonaneHCID 68529351123.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

9-(4-Benzyloxy-phenyl)-bicyclo[3.3.1]nonan-9-ol (4.7 g, 14.57 mmol) (prepared in accordance with the procedures set forth in Step 2 of Example 18) was dissolved in EtOH (150 mL) after which concentrated hydrochloric acid (15 mL) was added. This mixture was stirred at 50° C. overnight. The solvent was removed under reduced pressure. Water (50 mL) was added. The mixture was basified with aqueous ammonia and extracted three times with EtOAc. The organic phase was dried and concentrated to provide the title compound (5.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642603B2
Source datasetuspto-grants-2014_02
ORD IDord-73011340c21b43668ee6c3df638197a1
Source noteuspto-grants-2014_02