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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237759Generated: October 25, 2026

1-(4-Benzyloxy-phenyl)-3,3-dimethyl-cyclohexanol → 1-Benzyloxy-4-(3,3-dimethyl-cyclohex-1-enyl)-benzene

https://huagongshe.com/reaction/237759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Benzyloxy-phenyl)-3,3-dimethyl-cyclohexanolHCID 68523959—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product1-Benzyloxy-4-(3,3-dimethyl-cyclohex-1-enyl)-benzeneHCID 6852470892.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

1-(4-Benzyloxy-phenyl)-3,3-dimethyl-cyclohexanol (5.08 g, 16.4 mmol) was dissolved in EtOH (80 mL) after which concentrated hydrochloric acid (8 mL) was added. This mixture was stirred at 50° C. for 1.5 hours. The solvent was removed under reduced pressure. Water (15 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 as a yellow solid 4.43 g as a mixture of isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642603B2
Source datasetuspto-grants-2014_02
ORD IDord-0abd5aa8aad74627a470f8b01f77990a
Source noteuspto-grants-2014_02