Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129068생성일: 2026년 10월 25일
Salicylamide → o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide
https://huagongshe.com/reaction/129068
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Salicylamide | HCID 5147 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| 반응물 | 3-Hexyl-4-((R)-2-hydroxytridecyl)-2-oxetanone, (3S,4S)- | HCID 10428248 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide | HCID 54133504 | 49.5% |
반응 단계
1.1 g of (3S,4S)-3-hexyl-4-[(R)-2-hydroxytridecyl]-2-oxetanone, 1.6 g of triphenylphosphine, 0.825 g of salicylamide and 3 g of molecular sieve (4 Å) were treated with 20 ml of THF and cooled to 0° C. Thereupon, 1.4 g of di-t-butyl azodicarboxylate were added. After warming to room temperature and stirring the reaction mixture was concentrated and the residue was partitioned between methanol/water (70:30) and hexane and extracted with hexane. The hexane phase was dried and concentrated and the residue was chromatographed on silica gel with hexane/ethyl acetate (4:1). There were obtained 0.727 g of o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide, MS: 474 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05466708 |
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| 출처 데이터셋 | uspto-grants-1995_11 |
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| ORD ID | ord-5ec19bf755b94c5ca8e7a8d5d56850b2 |
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| 출처 메모 | uspto-grants-1995_11 |
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