HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanophenol → HCID 178456380, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | HCID 178456387 | HCID 178456387 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178456380 | HCID 178456380 | — |
Reaction Steps
To a mixture of 1.0 g (3.93 mmol) of cis-(4-isopropyl-piperazin-1-yl)-(4-hydroxy-cyclohexyl)-methanone, 0.515 g (4.3 mmol) of 4-cyanophenol, 1.28 g (4.88 mmol) of triphenylphisphine in 6 ml THF, 1.11 g (4.82 mmol) of di-tert-butyl azodicarboxylate in 6 ml of THF was added at 0° C., and stirred for 72 hr at room temperature. After evaporation, the residue was purified by column chromatography on silica gel eluting with cyclohexane and ethyl acetate=from 1:1 to 1:3, then dichloromethane and methanol=19:1. The combined product fractions were evaporated to dryness to yield 0.26 g (19% yields) of the titled compound. MS (m/e): 356.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544683B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-e5f28192823648eb9f4975bb5c2d4aa7 |
| Source note | uspto-grants-2009_06 |