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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754832Generated: October 28, 2026

Ethanol → 4-(Docosyloxy)-alpha-[4-(docosyloxy)phenyl]benzenemethanamine

https://huagongshe.com/reaction/1754832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl di(4-docosoxyphenyl)methylcarbamateHCID 86646200—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4-(Docosyloxy)-alpha-[4-(docosyloxy)phenyl]benzenemethanamineHCID 6657530598%

Reaction Conditions

Temperature100 °C

Reaction Steps

To crude crystals (31.9 g) of ethyl di(4-docosoxyphenyl)methylcarbamate were added toluene (300 mL), ethanol (200 mL) and sodium hydroxide (4.2 g, 105 mmol), and the mixture was refluxed under stirring at 100° C. Sodium hydroxide (total 9.8 g, 245 mmol) was added, and the mixture was stirred for 16 hr. The reaction mixture was cooled to room temperature, and water (300 mL), hexane (200 mL) and ethyl acetate (200 mL) were added for partitioning. The aqueous layer was discarded, and the organic layer and precipitated crystals were washed with water (300 mL×2). The organic layer and crystals were recovered. The solvent was evaporated under reduced pressure. To the residue were added water (150 mL) and acetonitrile (150 mL) to allow crystallization. The crystals were collected by filtration and thoroughly washed with water and acetonitrile to give di(4-docosoxyphenyl)methylamine (28.1 g, 33.7 mmol, 98% vs —OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169187B2
Source datasetuspto-grants-2015_10
ORD IDord-09cf9330e0384d5ea18c1e5014cc7b54
Source noteuspto-grants-2015_10