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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735876Generated: October 30, 2026

1-Tetradecyne → Ethyl oxo{(4-tetradec-1-ynylbenzyl)[4-(trifluoromethyl)benzyl]amino}acetate

https://huagongshe.com/reaction/735876

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-TetradecyneHCID 69823—
ReactantEthyl{(4-bromobenzyl)[4-(trifluoromethyl)benzyl]amino}(oxo)acetateHCID 67186610—
Catalystcopper(I) bromideHCID 24593—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventHydrochloric AcidHCID 313—
SolventTriethylamineHCID 8471—
ProductEthyl oxo{(4-tetradec-1-ynylbenzyl)[4-(trifluoromethyl)benzyl]amino}acetateHCID 6718789750%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of ethyl{(4-bromobenzyl)[4-(trifluoromethyl)benzyl]amino}(oxo)acetate (100 mg, 0.23 mmol), 1-tetradecyne (66 mg, 0.34 mmol), copper(I) bromide (4.5 mg, 0.031 mmol) and palladium tetrakis(triphenylphosphine) (11 mg, 0.0095 mmol) in Et3N (1 mL) was heated at 90° C. for 75 min. After cooling to rt, the reaction mixture was diluted with an aqueous HCl solution (1N, 10 mL) and extracted with Et2O (2×20 mL). The combined organic layers were dried over MgSO4 and the solvent was removed under reduce pressure. The residue was purified by flash chromatography (cyclohex./Et2O 4:1) to give the title compound as yellow oil (63 mg, 50%). 1H NMR (CDCl3, 300 MHz) δ 7.61 (m, 2H), 7.33 (m, 4H), 7.14 (m, 2H), 4.51 (s, 1H), 4.47 (s, 1H), 4.34 (m, 4H), 2.40 (m, 2H), 1.58-1.26 (m, 23H), 0.88 (m, 3H). HPLC (Condition A), Rt: 8.21 min (HPLC purity: 99.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592477B2
Source datasetuspto-grants-2009_09
ORD IDord-e40195fd509e4838b0f8975d02241470
Source noteuspto-grants-2009_09