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HRID 1012933作成日:2026年10月26日

rac-tert-butyl N-[(1r,4r)-4-formylcyclohexyl]carbamate → HCID 178489240、化合物

https://huagongshe.com/reaction/1012933

反応式

関与物質

役割名称HCID仕込み量
反応物rac-tert-butyl N-[(1r,4r)-4-formylcyclohexyl]carbamateHCID 11020615—
反応物4-Methoxy-1,3-benzothiazoleHCID 12631858—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178489240HCID 17848924053%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981886B2
出典データセットuspto-grants-2011_07
ORD IDord-728534994fab4e25b1ea419fa9a3127e
出典メモuspto-grants-2011_07