HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethynyltributyltin → HCID 59164456, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethynyltributyltin | HCID 621176 | — |
| Reactant | Methyl 2-amino-5-iodo-4-(trifluoromethyl)benzoate | HCID 53436880 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59164456 | HCID 59164456 | 69% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a solution of 2-amino-5-iodo-4-trifluoromethyl-benzoic acid methyl ester (1.5 g, 4.35 mmol) in dioxane (80 mL) were added tributyl(ethynyl)tin (1.4 mL, 4.78 mmol) and (Ph3P)4Pd (251.2 mg, 0.217 mmol) and the mixture was heated to 120° C. for 1.5 h. After cooling to r.t., the solvent was removed in vacuo and the residue was purified by two successive flash chromatographies (150 g silica gel, hexanes→DCM:hexanes (3:7 to 1:1) and then (50 g silica gel, hexanes→EtOAc:hexanes (1:9)) to provide the title compound (730 mg, 69%) as a beige-orange solid. API-ES: m/z 244 [M+H]+, rt 5.14 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07655666B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-06236f26f9654c7581bb5d31d1487427 |
| Source note | uspto-grants-2010_02 |