HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylcyclohexanol → HCID 178422868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylcyclohexanol | HCID 7391 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 6-Hydroxy-2-methylquinoline | HCID 594395 | — |
| Product | HCID 178422868 | HCID 178422868 | 56% |
Reaction Steps
To a solution of 2-Methyl-quinolin-6-ol (4.13 g, 0.0259 mol), c is 4-tert-Butyl-cyclohexanol (4.86 g, 0.0311 mol) and triphenylphosphine (9.53 g, 0.0363 mol; Supplier=Aldrich) in tetrahydrofuran (100 mL, 1 mol; Supplier=Acros), cooled in an ice bath, was added diisopropyl azodicarboxylate (7.61 mL, 0.0363 mol; Supplier=Acros) in Tetrahydrofuran (10 mL, 0.1 mol; Supplier=Acros). The reaction mixture was stirred for 72 h allowing to reach room temperature. The solvent was removed under reduced pressure and the residue was taken up in methylene chloride, adsorbed onto silica gel and purified by flash chromatography (0-30% ethyl acetate in hexanes) to give the title compound in 56% yield. ESI-MS (M+H+): 298.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802659B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-a88a55e1951a4c48b04c67ee84168a78 |
| Source note | uspto-grants-2014_08 |