関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Tert-Butylphenol | HCID 6923 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | N-Methylformanilide | HCID 66737 | — |
| 生成物 | 3-(tert-Butyl)-4-hydroxybenzaldehyde | HCID 3017618 | 22.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05731336 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-2b92740c81364c30af7dcfcac8c1abbd |
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| 出典メモ | uspto-grants-1998_03 |
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