참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | Hexylresorcinol | HCID 3610 | — |
| 반응물 | 2,6-Dimethylol-p-cresol | HCID 7039 | — |
| 반응물 | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2,6-Bis(2,4-dihydroxy-5-hexylbenzyl)-4-methylphenol | HCID 18792547 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06051358 |
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| 출처 데이터셋 | uspto-grants-2000_04 |
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| ORD ID | ord-c747984da85140ada52d871b3565a4df |
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| 출처 메모 | uspto-grants-2000_04 |
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