HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 1-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]cyclobutanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| 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 | 1-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]cyclobutanecarbonitrile | HCID 21990946 | — |
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 (250 mg, 0.95 mmol) was reacted with 1,3-Dibromopropane (120 μL, 1.1 mmol) to afford the desired 1-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]cyclobutanecarbonitrile as a colorless solid: 1H NMR (CDCl3, 300 MHz) δ 7.89–7.87 (m, 3H), 7.62–7.55 (m, 1H) 7.39–7.36 (m, 2H), 7.32–7.26 (m, 1H), 4.05 (s, 3H), 2.90–2.83 (m, 2H), 2.67–2.47 (m, 4H). MS (ESI) 305 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087601B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-aca996cf3f944717aae7a25cfe9fad93 |
| Source note | uspto-grants-2006_08 |