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rac-tert-butyl N-[(1r,4r)-4-formylcyclohexyl]carbamate → HCID 178489240、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | rac-tert-butyl N-[(1r,4r)-4-formylcyclohexyl]carbamate | HCID 11020615 | — |
| 反応物 | 4-Methoxy-1,3-benzothiazole | HCID 12631858 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | HCID 178489240 | HCID 178489240 | 53% |
反応手順
To a solution of 4-methoxy-benzothiazole (1.65 g, 10 mmol) in THF (50 ml) was added dropwise n-BuLi (2.5M in hexanes, 4 ml) so that the temperature did not exceed −70° C. The brown solution was stirred at this temperature for 15 min before dropwise addition of a solution of (4-formyl-cyclohexyl)-carbamic acid tert-butyl ester (1.14 g, 5 mmol) in THF (10 ml). The temperature was kept below −70° C. The brown solution was then gradually allowed to reach RT (over 3 h). The reaction mixture was quenched with saturated NH4Cl solution and extracted with EtOAc. The organic layer was washed with brine and dried over MgSO4 and concentrated under reduced pressure. The product was crystallised from ether to give 1.04 g (53%) of a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07981886B2 |
| 出典データセット | uspto-grants-2011_07 |
| ORD ID | ord-728534994fab4e25b1ea419fa9a3127e |
| 出典メモ | uspto-grants-2011_07 |