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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227073Generated: October 25, 2026

Ethyl Acetate → [2-[4-(Tetradecyloxy)phenyl]ethyl]aminobenzenemethanol

https://huagongshe.com/reaction/2227073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium SulfateHCID 24436—
ReactantEthyl 3-[[[4-(tetradecyloxy)phenyl]acetyl]amino]benzoateHCID 15030160—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product[2-[4-(Tetradecyloxy)phenyl]ethyl]aminobenzenemethanolHCID 86745967—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 42.36 ml of 1 molar lithium aluminum hydride in ether is added dropwise under argon over 20 minutes a solution of ethyl 3-[[[4-(tetradecyloxy)phenyl]acetyl]amino]benzoate in 50 ml of ether and 50 ml of tetrahydrofuran. The mixture is refluxed for 3 hours, cooled to 0° C. and ethyl acetate added. Saturated sodium sulfate is added followed by ether. The mixture is filtered and the cake washed with ether. The filtrate is evaporated and the residue chromatographed on silica gel using 9:1 chloroform:ethyl acetate. The product fractions are combined and evaporated to a residue which is crystallized from hexane to give 4.5 g of the desired product as a white solid, m.p. 67°-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350759
Source datasetuspto-grants-1994_09
ORD IDord-1022f5025b36415fa2056ee30aa522ca
Source noteuspto-grants-1994_09