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Boron trifluoride etherate → N-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | Diazomethane | HCID 9550 | — |
| 反応物 | N-p-methoxybenzyloxycarbonyl-D-serine benzyl ester | HCID 13652495 | — |
| 反応物 | Acetone cardice | HCID 18522661 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl ester | HCID 13652497 | 70% |
反応手順
The N-p-methoxybenzyloxycarbonyl-D-serine benzyl ester (720 mg, 2.00 mmol) is dissolved in dry dichloromethane (20 ml) and the solution cooled to dry ice/acetone. Boron trifluoride etherate (100 μl) is added followed by the portionwise addition of diazomethane (30 mmol in 20 ml CH2Cl2). After about 30 minutes the solution is filtered and washed once with water (10 ml), then dried (MgSO4) and evaporated to dryness. The resulting residue is chromatographed on silica gel using chloroform as eluant to give the pure title compound as an oil (520 mg, 70%) which crystallises on standing to give a colourless solid of m.p. 68°-69° C.; [α]D20 -1.3° (c 4.0, CHCl3).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04722924 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-3d9fe4eea0d14c78998610d953418f18 |
| 出典メモ | uspto-grants-1988_02 |