HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Biphenyl-4-yl-2,5-dimethoxytetrahydrofuran → 4'-(2,5-Dimethoxytetrahydrofuran-3-yl)-biphenyl-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Biphenyl-4-yl-2,5-dimethoxytetrahydrofuran | HCID 18380326 | — |
| Reactant | 4'-(2,5-Dimethoxy-2,5-dihydro-furan-3-yl)-biphenyl-4-carbonitrile | HCID 18380359 | — |
| Product | 4'-(2,5-Dimethoxytetrahydrofuran-3-yl)-biphenyl-4-carbonitrile | HCID 18380402 | 99.3% |
Reaction Steps
As described in Example 1(a) for the preparation of 3-biphenyl-4-yl-2,5-dimethoxy-tetrahydrofuran, 4′-(2,5-dimethoxy-2,5-dihydro-furan-3-yl)-biphenyl-4-carbonitrile (260 mg, 0.846 mmol) was reduced in 2 hours to give 260 mg (99%) of 4′-(2,5-dimethoxy-tetrahydrofuran-3-yl)-biphenyl-4-carbonitrile as a white solid, mp 149-50° C., which was used without firther purification. 1H NMR (CDCl3): δ 7.78-7.26 (m, 8H), 5.30-5.00 (m, 2H), 3.52-3.22 (m, 6H), 2.78-2.00 (m, 3H). IR (KBr): 2910, 2220. 1606, 1498, 1448, 1380, 1224, 1190 cm−1. Anal. Calculated for C19H19NO3•0.3 H2O: C, 72.28; H, 6.28; N, 4.45. Found: C, 72.28; H, 6.19; N, 4.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174915B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-ac121a1fca35493486158f04c0ba35d2 |
| Source note | uspto-grants-2001_01 |