참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 3037556 | — |
| 반응물 | Sodium dodecylbenzene sulphonate | HCID 57371080 | — |
| 촉매 | Hexadecyltrimethylammonium chloride | HCID 8154 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-Chloromethylfurfural | HCID 74191 | — |
반응 단계
To the same three-necked flask as in Example 1 were added 5 g (0.028 mole) of a commercially available D-(+)-galactose and two kinds of surface active agent, i.e., 89.6 mg (0.00028 mole) of cetyltrimethylammonium chloride and 97.6 mg (0.00028 mole) of sodium laurylbenzenesulfonate. Then, 30 ml of toluene was added thereto and the mixture was stirred to make a suspension. Thereafter, about 6 ml of 35% aqueous hydrochloric acid was added dropwise from a dropping funnel over about 1 hour. A slight excess of hydrogen chloride was then slowly passed therethrough at 50° C. over 3 hours with stirring. After stirring was continued for a further 5 hours, the reaction solution was diluted with a little water and filtered through Celite while being washed with toluene. The toluene layer was neutralized, dried and concentrated to obtain about 1.9 g (theoretical yield 4.01 g) of 5-chloromethylfurfural as a crude product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04154744 |
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| 출처 데이터셋 | uspto-grants-1979_05 |
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| ORD ID | ord-37b182d5d2eb41d79c8e5f2a89c4a45a |
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| 출처 메모 | uspto-grants-1979_05 |
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