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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754830Generated: October 28, 2026

Ethanol → {(4-Methoxy-phenyl)-[4-(3,4,5-tris-octadecyloxy-cyclohexylmethoxy)-phenyl]-methyl}-amine

https://huagongshe.com/reaction/1754830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl {(4-methoxy-phenyl)-[4-(3,4,5-tris-octadecyloxy-cyclohexylmethoxy)-phenyl]-methyl}-carbamateHCID 59510358—
SolventTolueneHCID 1140—
Product{(4-Methoxy-phenyl)-[4-(3,4,5-tris-octadecyloxy-cyclohexylmethoxy)-phenyl]-methyl}-amineHCID 46935395100%

Reaction Conditions

Temperature100 °C

Reaction Steps

To crude crystals (127 mg) of ethyl{(4-methoxy-phenyl)-[4-(3,4,5-tris-octadecyloxy-cyclohexylmethoxy)-phenyl]-methyl}-carbamate were added toluene (2 mL), ethanol (2 mL) and sodium hydroxide (21 mg, 525 μmol) and the mixture was stirred at 100° C. for 2 hr. The reaction mixture was cooled to room temperature, toluene (2 mL) was added, and washed with water (4 mL×3 times) to allow partitioning. The organic layer was evaporated, and the residue was crystallized from acetonitrile (5 mL) to give {(4-methoxy-phenyl)-[4-(3,4,5-tris-octadecyloxy-cyclohexylmethoxy)-phenyl]-methyl}-amine (123 mg, 100% vs —OH form).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169187B2
Source datasetuspto-grants-2015_10
ORD IDord-530ae4295dcc4fc8b47b4b53ab5e902d
Source noteuspto-grants-2015_10