HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dibromobutane → Diethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | Diethyl 5-(cyanomethyl)benzene-1,3-dioate | HCID 59709094 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioate | HCID 67318465 | — |
Reaction Steps
To a solution of diethyl 5-(cyanomethyl)benzene-1,3-dioate (500 mg, 1.9 mmol) in 18.6 mL THF was added potassium bis(trimethylsilyl)amide (1.1 g, 5.7 mmol) and the reaction was stirred at rt for 5 min. 1,4-Dibromobutane (0.25 mL, 2.1 mmol) was added, the mixture was stirred for 45 min and then quenched with 1N HCl. Ethyl acetate was added, the layers separated and the organic layer was washed with water and brine. Drying, solvent evaporation and flash chromatography (silica gel, 0-15% EtOAc/hexanes) gave diethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioate. 1H NMR (400 MHz, CDCl3) δ 8.63 (m, 1H), 8.31 (m, 2H), 4.43 (q, J=7.1 Hz, 4H), 2.56 (m, 2H), 2.14-1.99 (m, 6H), 1.43 (t, J=7.1 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354942B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-bb72fc4e9607484a98dd475c32ece0c3 |
| Source note | uspto-grants-2008_04 |