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HRID 2951作成日:2026年10月25日

2-Tert-Butylphenol → 3-(tert-Butyl)-4-hydroxybenzaldehyde

https://huagongshe.com/reaction/2951

反応式

関与物質

役割名称HCID仕込み量
反応物2-Tert-ButylphenolHCID 6923—
反応物Phosphorus oxychlorideHCID 24813—
反応物N-MethylformanilideHCID 66737—
生成物3-(tert-Butyl)-4-hydroxybenzaldehydeHCID 301761822.6%

反応手順

Into 101.5 g of N-methylformanilide was added dropwise with cooling 107 g of phosphoryl chloride over a period of 15 minutes. The mixture was allowed to warm to room temperature and stirred for 70 minutes. 67.5 g of ortho-t-butylphenol was added and stirred for about 45 minutes after which the mixture was heated to about 50°-60° C. and allowed to stir for 4.5 hours. The reaction mixture was poured into a volume of crushed ice and extracted with chloroform. The aqueous layer was separated and washed again with chloroform. The chloroform layers were combined and extracted with 2000 ml of a 5% potassium hydroxide solution. The aqueous potassium hydroxide layer was separated and added to 1000 ml of chloroform. The pH of the resulting two-phase mixture was adjusted to 3 with concentrated hydrochloric acid with stirring. The resultant layers were separated and the aqueous layer was again extracted with chloroform and dried over sodium sulfate overnight to give 18.1 g of the desired subtitled intermediate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731336
出典データセットuspto-grants-1998_03
ORD IDord-2b92740c81364c30af7dcfcac8c1abbd
出典メモuspto-grants-1998_03