HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704956Generated: October 31, 2026
1-[2-Chloro-4-(4-chlorophenoxy)phenyl]-2-(1H-1,2,4-triazol-1-yl)ethanone → HCID 71226383, compound
https://huagongshe.com/reaction/704956
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-[2-Chloro-4-(4-chlorophenoxy)phenyl]-2-(1H-1,2,4-triazol-1-yl)ethanone | HCID 15753778 | — |
| Reactant | HCID 178419101 | HCID 178419101 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71226383 | HCID 71226383 | — |
Reaction Steps
To a solution of the above-mentioned ethanone (75.5 g, 216.8 mmol) dissolved in THF (450 mL) was added a solution of LaCl3.2LiCl (395.9 mL, 0.6 M in THF) at room temperature and stirred for 1 hour. The resulting solution was added dropwise to 1-propynylmagnesium bromide (650.5 mL, 0.5M in THF) at room temperature. After 1 hour at room temperature, the resulting mixture was quenched with a 10% aqueous solution of HCl and extracted with MTBE. The organic phase was washed with brine, dried and evaporated. The crude compound was stirred in a solution of MTBE/diisopropylether and filtrated to eliminate the starting material. The mother liquors were evaporated and purified on silica gel to give the title compound as a beige solid (31.1 g, HPLC-MS2 Rt=1.15 min, masse=388, m.p=137° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09173402B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-2fef54e7b6a146babab8615a9705bb57 |
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| Source note | uspto-grants-2015_11 |
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