化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → 2-Formyl-3-(tert-butyldimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 反応物 | 2-Formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid allyl ester | HCID 53735263 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-Formyl-3-(tert-butyldimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl ester | HCID 53812279 | 93.8% |
反応手順
To a solution of 15 g of 2-formyl-3-hydroxy -5-methoxy-6-methylbenzoic acid allyl ester in 0.12 l of N,N-dimethylformamide were added 13.8 g of tert-butyl-dimethylchlorosilane and 12.0 g of triethylamine. The mixture was stirred for 3 h at room temperature and then evaporated in vacuo. The residue was taken up in 0.4 l of ethyl acetate and the solution was washed successively with 1N hydrochloric acid, water and brine. The organic layer was dried over sodium sulfate. The solvent was evaporated in vacuo and the solid residue was recrystallized from hexane to give 20.5 g of 2-formyl-3-(tert-butyl-dimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl ester as white crystals of m.p. 94°-95° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05589473 |
| 出典データセット | uspto-grants-1996_12 |
| ORD ID | ord-3f38b76d913f4cea9dcc0fe7b75e509f |
| 出典メモ | uspto-grants-1996_12 |