関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | tert-Butyl methyl ether | HCID 15413 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Methyl 2-hydroxy-5-methoxybenzoate | HCID 4072341 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 生成物 | Benzoic acid, 3-bromo-2-hydroxy-5-methoxy-, methyl ester | HCID 11184546 | 82.5% |
反応手順
In the course of from 30 to 45 minutes, at 20°, with stirring, 43.9 g of bromine are added dropwise to a solution of 45.9 g of 2-hydroxy-5-methoxy-benzoic acid methyl ester in 125 ml of heptane. The reaction mixture is then stirred for a further 3 to 4 hours, then diluted with 110 ml of water and stirred for a further one hour and then 295 ml of heptane and 46 ml of tert-butyl methyl ether are added thereto. The mixture is then heated to from 50° to 55° and the aqueous phase is separated off. The organic phase is extracted twice with 114 ml of water each time and cooled to -20°. The crystals which precipitate are filtered off and dried under a high vacuum. 3-Bromo-2-hydroxy-5-methoxy-benzoic acid methyl ester is thus obtained; yield 82.5% of the theoretical yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05290939 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-a893f363e49043b88b78e74c554c5397 |
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| 出典メモ | uspto-grants-1994_03 |
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