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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

반응식

참여 물질

역할이름HCID투입량
반응물SalicylamideHCID 5147—
반응물TriphenylphosphineHCID 11776—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물3-Hexyl-4-((R)-2-hydroxytridecyl)-2-oxetanone, (3S,4S)-HCID 10428248—
용매TetrahydrofuranHCID 8028—
생성물o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamideHCID 5413350449.5%

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05466708
출처 데이터셋uspto-grants-1995_11
ORD IDord-5ec19bf755b94c5ca8e7a8d5d56850b2
출처 메모uspto-grants-1995_11