HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 14496321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 14512984 | HCID 14512984 | — |
| Reactant | HCID 178418435 | HCID 178418435 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14496321 | HCID 14496321 | 95% |
Reaction Steps
12.09 g (0.04 mol) of 4'-acetyl-4-benzyloxybiphenyl (VII-23), 40 ml of tetrahydrofuran and 10 ml of methanol were supplied into a four-necked flask provided with a stirrer and a thermometer. Then 1.51 g (0.4 mol) of sodium boron hydride was added at 15°-25° C. over a period of 2 hours. The mixture was kept at the same temperature for 5 hours, then poured into ice-water and extracted with 50 ml of chloroform. The organic layer was concentrated under reduced pressure to give 11.0 g (95% yield) of 4-benzyloxy-4'-(1-hydroxyethyl)biphenyl (VI-23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985590 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-bca63a586eed4d13bad98483664ffcfe |
| Source note | uspto-grants-1991_01 |