HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylfuran → 2,5-Dihydro-2,5-dimethoxy-3-phenylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylfuran | HCID 518802 | — |
| Reactant | 3-Biphenyl-4-yl-2,5-dihydro-2,5-dimethoxyfuran | HCID 18380352 | — |
| Product | 2,5-Dihydro-2,5-dimethoxy-3-phenylfuran | HCID 18380367 | 82% |
Reaction Steps
According to the procedure described in Example 1(a) for the preparation of 3-biphenyl-4-yl-2,5-dihydro-2,5-dimethoxyfuran, 3-phenylfuran (see Pridgen, L. N.; Jones, S. S. J. Org. Chem. 1982, 47, 1590-1592 and Yang, Y.; Wong, H. N. C. Tetrahedron 1994, 32, 9583-9608; 848 mg, 5.89 mmol) provided 1.00 g (82%) of 2,5-dihydro-2,5-dimethoxy-3-phenylfuran as a yellow oil, which was an approximately 80:20 mixture of diastereomers by 1H NMR and used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06306892B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-6c95fa0a61fe4f2ea66187116e6a16c9 |
| Source note | uspto-grants-2001_10 |