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Ethyl Acetate → 1-cyclopentyl N-[3-(bromomethyl)benzyl]-2-methylalaninate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | 3-(Bromomethyl)benzaldehyde | HCID 7127825 | — |
| 反応物 | alpha,alpha-Dimethylglycine cyclopentyl ester | HCID 59622352 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | 1-cyclopentyl N-[3-(bromomethyl)benzyl]-2-methylalaninate | HCID 86686427 | 39.2% |
反応手順
To a solution of 3-(bromomethyl)-benzaldehyde (0.503 g, 2.52 mmol) in dichloroethane (20 mL) was added α,α-dimethylglycine cyclopentyl ester (0.893 g, 5.2 mmol) and sodium triacetoxyborohydride (1.47 g, 6.9 mmol). The mixture was stirred at room temperature for 3 hours, then poured into ethyl acetate (200 mL) and washed with saturated ammonium chloride solution (3 times 50 mL). The organic fraction was dried (MgSO4), concentrated and purified by flash column chromatography (SiO2, 7:3 heptane:ethyl acetate) to yield the desired product (0.350 g, 39% yield). LC/MS: m/z 354/356 [M+H]+
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09321718B2 |
| 出典データセット | uspto-grants-2016_04 |
| ORD ID | ord-12968c7296d848ee993da33f3dbf7c2e |
| 出典メモ | uspto-grants-2016_04 |