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HRID 517937作成日:2026年10月25日

Triphenylphosphine → Tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/517937

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物o-Cresol, 4-bromo-alpha,alpha,alpha-trifluoro-HCID 142784—
反応物1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
反応物Diisopropyl azodicarboxylateHCID 5363146—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylateHCID 67294273—

反応手順

DIAD (33.5 g) was added dropwise to the solution of triphenylphosphine (43.5 g), 4-bromo-2-trifluoromethylphenol (40 g) and tert-butyl 4-(2-hydroxyethyl)-piperidine-1-carboxylate (31.7 g) in DCM (200 ml) at 0° C. during 15 minutes. The mixture was then stirred at room temperature for 20 hours. After removal of DCM under reduced pressure, to the residue was added ether (100 ml) and heptane (300 ml), solid was then filtered off. Filtrate was then washed with 1M sodium hydroxide (100 ml×3). Organic layer dried over sodium sulphate, solvent removed under vacuum, residue was then columned on silica gel using heptane:EtOAc (5:1) as eluant to give tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate as a colorless oil as product (61.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115126B2
出典データセットuspto-grants-2015_08
ORD IDord-397246aa07b34753bc7c02ee9f38aeec
出典メモuspto-grants-2015_08