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HRID 485957作成日:2026年10月26日

1,2-Dichlorobenzene → Benzene, 1,2-bis(phenylmethyl)-

https://huagongshe.com/reaction/485957

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichlorobenzeneHCID 7239—
反応物DibenzylHCID 7647—
反応物Benzene, 1-chloro-2-(phenylmethyl)-HCID 123431—
反応物HCID 178461630HCID 178461630—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Benzene, 1,2-bis(phenylmethyl)-HCID 1093416138.4%

反応手順

This Example illustrates the use of EtMgBr/[NitriphosCl]PF6 as an activator/catalyst to improve yield. To 2.00 g (13.61 mmoles) of o-dichlorobenzene, 0.050 g (0.065 mmoles) of [NitriphosCl]PF6 in 5 mL of ether at 0° C. was added 0.5 mL (1.5 mmoles) of 2.9M EtMgBr in ether. After stirring for 0.5 hrs, 30 mL of ether and 7.0 mL (14 mmoles) of 2M benzylMgCl in THF were added. The mixture was refluxed for 3 days and worked up as usual. After removing the solvent, the residue was distilled at 0.1 mm to initially remove 0.550 g (3.7 mmoles, 27%) of o-dichlorobenzene and then 1.482 g (bp: 68° to 83° C.) of a clear liquid was collected. 1H NMR spectrum in CDCl3 indicated a 10:1 ratio of 1-chloro-2-benzylbenzene to bibenzyl (representing 6.7 mmoles (67 % based on reacted o-dichlorobenzene) of 1-chloro-2-benzylbenzene and 0.67 mmoles of bibenzyl). The material that remained in the pot was chromatographed on silica gel eluted with 10% EtOAc/hexane to give 0.602 g (2.57 mmoles, 19%) of 1,2-dibenzylbenzene (mp: 61° to 67° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04538003
出典データセットuspto-grants-1985_08
ORD IDord-3aa0f4bbd4fe4f7aa0b802077bdc6964
出典メモuspto-grants-1985_08