HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Carbonate → Ethyl 2-(4-benzyloxyphenyl)cyanoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | 4-Benzyloxyphenylacetonitrile | HCID 522804 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-(4-benzyloxyphenyl)cyanoacetate | HCID 23001570 | 99.2% |
Reaction Steps
The 4-benzyloxybenzyl cyanide from step (450a)(3.2 g, 14.33 mmol), sodium ethoxide (1.07 g, 15.7 mmol), and diethyl carbonate (2.23 g, 18.9 mmol) were combined in toluene (100 mL), heated to reflux for 3 h, cooled to rt, and partitioned between ethyl acetate and 1 N HCl. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The crude was purified by chromatography on silica gel eluting hexane: ethyl acetate (80:20, v:v) to give ethyl 2-(4-benzyloxyphenyl)cyanoacetate (4.2 g, 99%) as an oil. MS (M+NH4)+ =313.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057336 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-cfecfa198e244158a2645819786085c1 |
| Source note | uspto-grants-2000_05 |