HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 5-Chloro-6-(1-isopropyl-piperidin-4-yloxy)-3-methyl-benzofuran-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Isopropylpiperidin-4-ol | HCID 79681 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | 5-Chloro-6-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 68724257 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-6-(1-isopropyl-piperidin-4-yloxy)-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 68723624 | 94.8% |
Reaction Steps
The above prepared 5-chloro-6-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester (0.700 g, 2.75 mmol) was dissolved in 12 mL of THF and treated successively at −10° C. with 1-isopropyl-piperidin-4-ol (0.551 g, 1.4 eq.), triphenylphosphine (1.001 g, 1.4 eq.) and DIAD (0.755 mL, 1.4 eq.), and the mixture then kept at ambient temperature for another 4 h. Pouring onto crashed ice/NH4Cl, twofold extraction with AcOEt, washing with water and brine, drying over magnesium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, NEt3/AcOEt=2/98), produced 0.990 g of the title compound as light yellow gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534788B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-0d504c4eecf64e069f6c3c3da0c24b7f |
| Source note | uspto-grants-2009_05 |