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Hydrochloric Acid → Ethyl 2-(4-benzyloxyphenyl)cyanoacetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Diethyl Carbonate | HCID 7766 | — |
| 反応物 | 4-Benzyloxyphenylacetonitrile | HCID 522804 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Ethyl 2-(4-benzyloxyphenyl)cyanoacetate | HCID 23001570 | 99.2% |
反応手順
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 partioned 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06610731B2 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-94741de82d734d9693cabe305f6d8d9d |
| 出典メモ | uspto-grants-2003_08 |