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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Tetradecyne | HCID 69823 | — |
| Reactant | Ethyl{(4-bromobenzyl)[4-(trifluoromethyl)benzyl]amino}(oxo)acetate | HCID 67186610 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl oxo{(4-tetradec-1-ynylbenzyl)[4-(trifluoromethyl)benzyl]amino}acetate | HCID 67187897 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592477B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-e40195fd509e4838b0f8975d02241470 |
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| Source note | uspto-grants-2009_09 |
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