HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464298Generated: October 26, 2026
Water → 5-(3-methoxyphenyl)-2-(3-pyridylmethyl)-1H-isoindole-1,3 (2H)-dione
https://huagongshe.com/reaction/1464298
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 57242191 | HCID 57242191 | — |
| Reactant | HCID 178490745 | HCID 178490745 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(3-methoxyphenyl)-2-(3-pyridylmethyl)-1H-isoindole-1,3 (2H)-dione | HCID 57269499 | — |
Reaction Steps
To a solution of 1.80 g of zinc chloride in 8.8 ml of tetrahydrofuran was added 8.8 ml of tetrahydrofuran solution (1.0M) of 3-methoxyphenylmagnesium bromide, and the resultant mixture was stirred at room temperature for 20 minutes. This solution was added to a mixture of 2.27 g of 2-(3-pyridylmethyl)-5-(trifluoromethanesulfonyloxy)-1H-isoindole-1,3 (2H)-dione, 27 mg of palladium acetate, 131 mg of 1,1'-bis (diphenylphosphino) ferrocene and 18 ml of tetrahydrofuran and stirred at room temperature for 17 hours. After finishing the reaction, the mixture was mixed with water under ice cooling and shaken with ethyl acetate. The organic layer was washed with water and saturated brine in order, dried over anhydrous magnesium sulfate and concentrated in vacuo. The resultant residue was chromatographed on a column of silica gel, eluting with ethyl acetate and hexane (1:3) to (1:1) to give 1.71 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05304556 |
|---|
| Source dataset | uspto-grants-1994_04 |
|---|
| ORD ID | ord-8c2cd815f7184bb6b969492900f3f7cc |
|---|
| Source note | uspto-grants-1994_04 |
|---|