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HRID 349741作成日:2026年10月26日

1,2-Dichloro-4-fluorobenzene → 4-(3,4-Dichlorophenoxy)-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/349741

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Dichloro-4-fluorobenzeneHCID 74028—
反応物Sodium BicarbonateHCID 516892—
反応物tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 9835508—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3,4-Dichlorophenoxy)-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl esterHCID 11212544—

反応手順

To a solution of potassium tert-butoxide (139.0 g, 1.24 mol) in THF (500 ml) was added a solution of the product of Step 1 (176.2 g, 0.62 mol) in THF (1000 ml). The reaction mixture was stirred 10 minutes before the additon of 3,4 dichlorofluorobenzene (122.8 g, 0.74 mol), this caused a green colouration that subsequently faded. The reaction mixture was then heated at reflux for 90 minutes. The reaction mixture was then cooled to room temperature before the addition of saturated NaHCO3 (1600 ml). The layers were separated and the organic layer stripped to leave an orange semi-solid. The solid was dissolved in DCM (1500 ml) and dried (MgSO4), filtered and the solvent removed. To the resultant solid was added methyl tert-butyl ether (MTBE) (54 ml) and iso-hexane (1000 ml) to give a slurry which was stirred overnight. The slurry was then filtered and washed with isohexane (200 ml) and the solid dried in vacuo at 50° C. to give the sub-titled compound as a pale powder, (211.6 g, 80%; MS: (M+H) 429).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179922B2
出典データセットuspto-grants-2007_02
ORD IDord-fa76b7452d9a43bf95ccd356985efa47
出典メモuspto-grants-2007_02