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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 741783생성일: 2026년 10월 26일

Hydrochloric Acid → Lauryl 3-[N-(1-Octyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-N-hydroxyamino]propionate

https://huagongshe.com/reaction/741783

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lauryl acrylateHCID 75084—
반응물1-Octyloxy-2,2,6,6-tetramethylpiperidin-4-one oximeHCID 22902698—
반응물HCID 178418361HCID 178418361—
촉매PlatinumHCID 23939—
용매MethanolHCID 887—
생성물Lauryl 3-[N-(1-Octyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-N-hydroxyamino]propionateHCID 2290271657.8%

반응 단계

A mixture of 1-octyloxy-2,2,6,6-tetramethylpiperidin-4-one oxime (10.0 g, 35.4 mmol) (a mixture of octyloxy isomers) 5.5 ml of concentrated hydrochloric acid and 130 ml of methanol is subjected to 3 atmospheres of hydrogen over 5% platinum on carbon for 18 hours. The reaction mixture is filtered through celite and then concentrated. The residue is partitioned between ethyl acetate and aqueous potassium carbonate. The organic layer is washed with water and brine, dried over anhydrous sodium sulfate and finally concentrated to a total volume of about 150 ml. Lauryl acrylate (7.7 g, 32 mmol ) is added. After a two-hour reaction time, the reaction mixture is concentrated and the crude product purified by flash chromatography on silica gel (9:1, hexane:ethyl acetate) to yield 10.0 g (52% yield) of a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05552464
출처 데이터셋uspto-grants-1996_09
ORD IDord-6edf92e84dbe4363b2dee818ac08c813
출처 메모uspto-grants-1996_09