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HRID 1493078作成日:2026年10月25日

Salicylamide → o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide

https://huagongshe.com/reaction/1493078

反応式

関与物質

役割名称HCID仕込み量
反応物SalicylamideHCID 5147—
反応物TriphenylphosphineHCID 11776—
反応物Di-tert-butyl azodicarboxylateHCID 97268—
反応物3-Hexyl-4-((R)-2-hydroxytridecyl)-2-oxetanone, (3S,4S)-HCID 10428248—
溶媒TetrahydrofuranHCID 8028—
生成物o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamideHCID 5413350449.5%

反応条件

温度0 °C

反応手順

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 (4Å) 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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05376674
出典データセットuspto-grants-1994_12
ORD IDord-32bbc7053aaa4bdb801f8859ed4d5129
出典メモuspto-grants-1994_12