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HRID 592120作成日:2026年10月25日

Acetonitrile → 1,2-Dibromo-3,4-dimethylbenzene

https://huagongshe.com/reaction/592120

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Ammonium BicarbonateHCID 14013—
反応物o-Bis(bromomethyl)benzeneHCID 66665—
反応物1,4-Bis(bromomethyl)benzeneHCID 69335—
反応物Benzene, 1,3-bis(bromomethyl)-HCID 69373—
反応物2,6-Bis(bromomethyl)pyridineHCID 603610—
反応物trans-1,4-Dibromo-2-buteneHCID 641245—
溶媒WaterHCID 962—
生成物1,2-Dibromo-3,4-dimethylbenzeneHCID 34343—

反応手順

A 100 mL flask is charged with acetonitrile (12 mL) and water (24 mL) and is degassed with argon for about 5 min. Linear peptide (0.01 mmole) and 200 mM ammonium bicarbonate (6 mL) are added followed by at least one peptide (0.012 mmole) such as, but not limited to, 1,3-bis(bromomethyl) benzene, 1,2-bis(bromomethyl)benzene, 1,4-bis(bromomethyl)benzene, 2,6-bis(bromomethyl)pyridine, (E)-1,4-dibromobut-2-ene. The reaction mixture is stirred under argon at room temperature for approximately 2 hours and monitored by LC-MS. After the reaction is complete, the reaction solution is frozen and lyophilized. HPLC purification of the crude lyophilized product followed by lyophilization of fractions containing pure peptide results in the final cyclized product as a white power.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238676B2
出典データセットuspto-grants-2016_01
ORD IDord-116fd473aadb431cb20d499af6636211
出典メモuspto-grants-2016_01