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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1732726생성일: 2026년 10월 25일

O-Xylene → HCID 86737387, 화합물

https://huagongshe.com/reaction/1732726

반응식

참여 물질

역할이름HCID투입량
반응물O-XyleneHCID 7237—
반응물4-Piperidinol, 2,2,6,6-tetramethyl-1-(phenylmethyl)-HCID 103602—
반응물1,2,2-Hexanetricarboxylic acid, triethyl esterHCID 12296885—
반응물HCID 178506930HCID 178506930—
용매EthanolHCID 702—
생성물HCID 86737387HCID 86737387—

반응 단계

30.2 g (0.1 mol) of triethyl hexane-1,2,2-tricarboxylate, 74.2 g (0.3 mol) of 1-benzyl-2,2,6,6-tetramethyl-4-hydroxypiperidine and 50 ml of xylene are warmed to 130° and mixed with 0.8 g of LiNH2. The ethanol formed is distilled off continuously. The solution is kept at the above temperature for 3 hours, so that it can then be kept at 150° for a further 2 hours. After cooling, the residue is taken up in toluene, a little glacial acetic acid is added to the solution and the latter is washed with H2O. After drying over Na2SO4, the solvent is distilled off in vacuo. Tris-(1-benzyl-2,2,6,6-tetramethyl-4-piperidinyl)hexane-1,2,2-tricarboxylate is obtained as a powdery residue. (Compound No. 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04238613
출처 데이터셋uspto-grants-1980_12
ORD IDord-f49222781930484c9ba96ee7d95aca35
출처 메모uspto-grants-1980_12