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HRID 399326作成日:2026年10月26日

2,6-Di-tert-butylphenol → 4-Bromo-2,6-di-tert-butylphenol

https://huagongshe.com/reaction/399326

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Di-tert-butylphenolHCID 31405—
反応物BROMINE CHLORIDE (BrCl)HCID 61697—
溶媒1,2-DichloroethaneHCID 11—
溶媒Diethyl EtherHCID 3283—
生成物4-Bromo-2,6-di-tert-butylphenolHCID 7082992%

反応手順

To a solution of 2,6-di-tert-butylphenol (2.06 g, 10 mmol) in EDC (50 mL) in a 200-mL round bottom flask, was added the stabilized BrCl brominating reagent (12 mL, about 11 mmol) dropwise, with stirring at room temperature. Initially, the orange reddish color of the reagent disappeared quickly. The color from the last 1 mL persisted for several minutes. The reaction mixture was allowed to stand for 30 minutes before being quenched with a few drops of sodium sulfite solution. After phase separation, it was diluted with EDC (50 mL), washed with water (100 mL) and dried (Na2SO4). The organic layer was concentrated under reduced pressure to afford a glue-like material. The material was redissolved in ether (10 mL) and after solvent removal, a crystalline solid 4-bromo-2,6-di-tert-butylphenol product (2.63 g, 92% recovered yield) was obtained in high purity (>98% by GC).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05817888
出典データセットuspto-grants-1998_10
ORD IDord-f83b1b5df26c4f0489d308504a235b0f
出典メモuspto-grants-1998_10