HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(2-Cyclopropylethynyl)-4-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Iodoanisole | HCID 69676 | — |
| Reactant | 1-Cyclopropylethynyl-4-methoxy-benzene Cyclopropylethyne | HCID 86603546 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Cyclopropylethynyl)-4-methoxybenzene | HCID 58609803 | 67% |
Reaction Steps
1-Cyclopropylethynyl-4-methoxy-benzene Cyclopropylethyne (15 g, 0.22 mol) was slowly added to a mixture of 4-iodoanisole (30 g, 0.13 mol), copper (I) iodide (1.2 g, 0.0063 mol), and triethylamine (30 g, 0.30 mol) in tetrahydrofuran (THF, 400 mL). After being stirred for 4 hours, the resulting precipitate was filtered and washed with THF. The combined filtrate was evaporated to dryness and the residue was purified by column chromatography to afford 1-cyclopropylethynyl-4-methoxy-benzene as a yellow oil (15 g, 0.087 mol, 67%). 1H NMR (CDCl3). 7.31 (d, J=8.8 Hz, 2 H), 6.80 (d, J=8.8 Hz, 2 H), 3.79 (s, 3 H), 1.43 (m, 1 H), 0.85 (m, 2 H), 0.78 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977322B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-80b7a2a876ca48b5a34f9ada27d1f223 |
| Source note | uspto-grants-2011_07 |