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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1073518생성일: 2026년 10월 27일

2-Chloropyridine → Pyriproxyfen

https://huagongshe.com/reaction/1073518

반응식

참여 물질

역할이름HCID투입량
반응물2-ChloropyridineHCID 7977—
반응물Sodium HydroxideHCID 14798—
반응물1-(4-Phenoxyphenoxy)propan-2-olHCID 10399568—
촉매Tetrabutylammonium BromideHCID 74236—
용매TolueneHCID 1140—
생성물PyriproxyfenHCID 9175371%

반응 단계

A mixture of 1-methyl-2-(4-phenoxyphenoxy)ethanol (2.0 g, 8.2 mmol), 2-chloropyridine (4.0 g, 35 mmol), flaked 95% sodium hydroxide (1 g, 24 mmol) and tetra-n-butylammonium bromide (0.13 g) was stirred at an inner temperature of 85° to 90° C. for 6 hours. After allowed to cool, toluene (10 g) was added thereto, and the resultant mixture was washed with water and extracted with 35% hydrochloric acid (5 g) twice. The hydrochloric acid layer was washed with toluene (10 g). A 10% aqueous sodium hydroxide solution was added thereto to make the mixture sufficiently basic. The basic mixture was further extracted with toluene (10 g) twice, and the toluene layer was washed with a 10% aqueous sodium hydroxide solution and a saturated aqueous sodium chloride solution in order and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was purified by silica gel column chromatography to give 2-[1-methyl- 2-(4-phenoxyphenoxy)ethoxy]pyridine (1.87 g) as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04970222
출처 데이터셋uspto-grants-1990_11
ORD IDord-9478d0c3a3944225adf0b02b98f51785
출처 메모uspto-grants-1990_11