関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | Hexylresorcinol | HCID 3610 | — |
| 反応物 | 2,6-Dimethylol-p-cresol | HCID 7039 | — |
| 反応物 | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2,6-Bis(2,4-dihydroxy-5-hexylbenzyl)-4-methylphenol | HCID 18792547 | — |
反応手順
To 500 ml flask was added 300 ml of methanol, 60 g of 4-hexylresorcinol and 16.9 g of 2,6-bis(hydroxymethyl)-4-methylphenol. 2.2 g of toluenesulfonic acid monohydrate was then added and the reaction solution heated at reflux for 20.5 hours. The warm reaction solution was slowly added, with agitation, to about 1.5 L of de-mineralized water containing about 1.3% hydrochloric acid. To the precipitate mixture an additional 20 ml of concentrated hydrochloric acid was added and mixed until the precipitate solidified. The crude product was collected on a filter, reduced to small pieces and air dried while gently warmed on a hot plate. To the crude product 200 ml of toluene was added and the mixture heated to about 85° C. The hot solution was filtered using a pre-heated Buchner funnel and the filtrate allowed to stand at room temperature. The crystals were collected on the filter, rinsed and slurred in 50 ml of cold toluene. After collection and drying about 16.5 g of product was obtained having a purity of about 95% as determined by HPLC.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06051358 |
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| 出典データセット | uspto-grants-2000_04 |
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| ORD ID | ord-c747984da85140ada52d871b3565a4df |
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| 出典メモ | uspto-grants-2000_04 |
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