HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propane, 2,2',2''-[methylidynetris(oxy)]tris- → HCID 18187329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propane, 2,2',2''-[methylidynetris(oxy)]tris- | HCID 78191 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 18187313 | HCID 18187313 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18187313 | HCID 18187313 | — |
| Product | HCID 18187329 | HCID 18187329 | 49% |
Reaction Steps
Method PP: To a stirred solution of 7-chloro-5-formyl-5-(1,1-difluoroethyl)-5,10-dihydrobenzo[b][1,8]naphthyridine (51) (619 mg, 2.005 mmol) in anhydrous triisopropyl orthoformate (30.0 mL, 134 mmol), anhydrous isopropanol (10 mL) and anhydrous methylene chloride (10 mL) at room temperature was added p-TsOH.H2O (763 mg, 4.010 mmol). After 18 h at room temperature, the reaction was quenched with saturated aqueous NaHCO3 (25 mL), and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. Flash chromatography (30%-40% EtOAc-hexane, gradient elution) afforded 53 (400 mg, 49% yield) as a yellow solid as well as 45% recovery of starting material 51 (280 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06593337B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-bf02564507c64935938e666056d77af7 |
| Source note | uspto-grants-2003_07 |