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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21691생성일: 2026년 10월 24일

Sodium Hydroxide → 2-chloro-6-(2,4,4-trimethypentyloxy)pyridine N-oxide

https://huagongshe.com/ko/reaction/21691

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2,4,4-Trimethylpentan-1-olHCID 85984—
반응물2,6-Dichloropyridine N-OxideHCID 817673—
용매Dimethyl SulfoxideHCID 679—
생성물2-chloro-6-(2,4,4-trimethypentyloxy)pyridine N-oxideHCID 88358226—

반응 단계

The 0.82 g (0.0050 moles) of 2,6-dichloropyridine N-oxide and 0.664 g (98%) (0.0050 moles) of 2,4,4-trimethyl-1-pentanol was reacted with 0.211 g (0.0050 moles) of ground sodium hydroxide in 8.2 ml of DMSO at 100° C. overnight to give 2-chloro-6-(2,4,4-trimethypentyloxy) pyridine N-oxide. It was reacted with 0.600 g (0.015 moles) of ground sodium hydroxide at 100° C. for 4.5 hours to give 1-hydroxy-6-(2,4,4-trimethylpentyloxy)pyridine-2(1H)-one. After cooling, it was added 74 ml of water and was adjusted with 6N HCl to pH 3. It was extracted with ethyl acetate (3×25 ml). The combined ethyl acetate extract was washed with a saturated sodium chloride solution (2×10 ml) and dried over sodium sulfate. The ethyl acetate extract was filtered and stripped in vacuo to give 1.08 g (90%). It was recrystallized from ethyl acetate and hexanes: mp 133.5°-134° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424435
출처 데이터셋uspto-grants-1995_06
ORD IDord-6f86b81f4a3249f8a11f4c5c52b2bf8d
출처 메모uspto-grants-1995_06