참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | 2,8-Dimethyl-1-oxa-8-azaspiro[4.5]decan-3-one | HCID 10176401 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Ammonia | HCID 222 | — |
| 생성물 | Tetradecane | HCID 12389 | — |
반응 단계
A mixture of 730 mg 2,8-dimethyl-1-oxa-8-azaspiro[4,5]-decan-3-one, 2.25 ml ethylene glycol, 836 mg p-toluenesulfonic acid monohydrate and 30 ml toluene was heated under reflux for 3 hours with a Dean-Strak azeotropic dehydration apparatus, and the reaction mixture was poured into 30 ml of an aqueous solution containing 1.26 g sodium becarbonate. The resulting mixture was extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography on silica gel eluted with a mixted solvent of chloroform/methanol/conc. ammonia (20:1:0.1 by volume) to give 640 mg of 10,14-dimethyl-1,4, 13-trioxa-10-azasprio[4.1.5.2]tetradecane as oil. It was dissolved in isopropanol, and a solution of maleic acid in isopropanol was added to convert it to the corresponding maleate, which was recrystallized from dichloromethane/ether.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | USRE034653 |
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| 출처 데이터셋 | uspto-grants-1994_07 |
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| ORD ID | ord-8c648554e77541a09bd315258677225c |
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| 출처 메모 | uspto-grants-1994_07 |
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