참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Trichloroacetyl chloride | HCID 6420 | — |
| 반응물 | 2,3-Dimethyl-4-propoxypyridine 1-oxide | HCID 15035537 | — |
| 용매 | Isopropyl Acetate | HCID 7915 | — |
| 생성물 | 2-Chloromethyl-3-methyl-4-propoxypyridine hydrochloride | HCID 21296003 | — |
반응 단계
A solution of 23 ml of trichloroacetyl chloride in 50 ml of isopropyl acetate is added dropwise during 1 hour to a solution, boiling at reflux under argon, of 13 g of 2,3-dimethyl-4-propoxypyridine 1-oxide in 250 ml of isopropyl acetate. At the beginning the reaction exhibits a very exothermic character. During the addition of the first mol equivalent of trichloroacetyl chloride a vigorous evolution of carbon dioxide is observed. The solution is subsequently stirred under argon for a further 15 minutes at reflux temperature (oil-bath 130° ), cooled to 10° with ice. treated with 100 ml of ether and stirred for 1 hour while cooling with ice. The crystalline precipitate which separates during the entire reaction is filtered off under suction and washed with ice-cold isopropyl acetate and ether. Crystalline reaction product can again be obtained from the mother liquor. The 2-chloromethyl-3-methyl-4-propoxypyridine hydrochloride obtained is processed directly.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04766133 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-3e8c259a6f7645cdae3e0abea5f224a9 |
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| 출처 메모 | uspto-grants-1988_08 |
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