HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 20308543, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20308544 | HCID 20308544 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20308543 | HCID 20308543 | — |
Reaction Steps
Sodium hydride (0.72g) was added to a solution of 7-hydroxy-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline (2.33g) in dry tetrahydrofuran (75 ml). Epibromohydrin (4.11 g) was added and the solution refluxed for 2 hr. until thin layer chromatography (alumina, chloroform-ether 1:5) showed the absence of starting phenol. Water (25ml) was added and the mixture extracted with ether. The combined ether layers were dried (MgSO4) and the solvent removed under reduced pressure. The oil was taken up in xylene (50 ml) and evaporated to dryness to give the title compound in quantitative yield. τ (CDCl3) 7.68 (3H,s), 7.55-7.0 (3H,m), 6.95-6.6 (2H,m), 6.4 (2H,s), 6.2-5.65 (3H,m), 3.5-3.1 (3H,m), 2.85 (5H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04113869 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-d63466b6881a4d618dc22696a93b7f7e |
| Source note | uspto-grants-1978_09 |