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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Ethyl 3-[[[4-(tetradecyloxy)phenyl]acetyl]amino]benzoate | HCID 15030160 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-[4-(Tetradecyloxy)phenyl]ethyl]aminobenzenemethanol | HCID 86745967 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05350759 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-1022f5025b36415fa2056ee30aa522ca |
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| Source note | uspto-grants-1994_09 |
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