HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Biphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Biphenyl | HCID 7095 | — |
Reaction Steps
1.31 g (3 mmol) of II-23 was mixed with 10 ml of tetrahydrofuran, 3 ml of toluene and 0.1 g of 2% Pd-carbon, and the mixture was subjected to catalytic hydrogenation in a hydrogen atmosphere. The reaction mixture was filtered to remove the catalyst and further treated and purified according to Example 21 to obtain 0.32 g (31% yield) of (+)-4-hydroxy-4'-(1-2's,3's-2-chloro-3-methylpentanoyl)ethyl)biphenyl. [α]D25 =+60° (c=1, CHCl3), m.p.=99°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985590 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-45f0d2f2be7c442d8b320bd0a663fc67 |
| Source note | uspto-grants-1991_01 |