HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 2-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]butanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 2-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]propanenitrile | HCID 10149373 | — |
| Reactant | 4-(1,3-Benzoxazol-2-yl)-2-methoxybenzonitrile | HCID 21990987 | — |
| Product | 2-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]butanenitrile | HCID 10171688 | — |
Reaction Steps
Utilizing the general procedure outlined in the synthesis of 2-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]propanenitrile, 4-(1,3-benzoxazol-2-yl)-2-methoxybenzonitrile (300 mg, 1.1 mmol) was reacted with iodoethane (90 μL, 1.1 mmol) to afford the desired 2-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]butanenitrile as a yellow solid: 1H NMR (CDCl3, 300 MHz) δ 7.87–7.84 (d, 1H), 7.79–7.74 (m, 2H), 7.59–7.53 (m, 2H), 7.37–7.34 (m, 2H), 4.22–4.17 (t, 1H), 3.97 (s, 3H), 1.95–1.89 (m, 2H), 1.13–1.08 (t, 3H). MS (ESI) 293 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087601B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-724a3c91a84f48bd9c3cc3b59fcaf0b0 |
| Source note | uspto-grants-2006_08 |