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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487033생성일: 2026년 10월 25일

Acetonitrile → 1-O-(2,4,8,10-Tetra-tert-butyl-dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl)-2,2'-methylenebis-(4,6-di-tert-butylphenol)

https://huagongshe.com/reaction/487033

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물2,2'-Methylenebis(4,6-di-tert-butylphenol)HCID 84391—
반응물3-Chloro-2,4,8,10-tetra-tert-butyl-dibenzo[d,f][1,3,2]dioxaphosphepinHCID 19096406—
용매TolueneHCID 1140—
생성물1-O-(2,4,8,10-Tetra-tert-butyl-dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl)-2,2'-methylenebis-(4,6-di-tert-butylphenol)HCID 1909640785%

반응 단계

Into a solution of 21.23 g (50 mmol) of 2,2'-methylenebis(4,6-di-tert-butylphenol) and 7 mL (50 mmol) of triethylamine in 200 mL of toluene is added dropwise a solution of 23.84 g (50 mmol) of 3-chloro-2,4,8,10-tetra-tert-butyl-dibenzo[d,f][1,3,2]dioxaphosphepin in 100 mL of toluene at ambient temperature. After 20 hours of stirring at ambient temperature, the reaction mass is filtered to remove triethylamine hydrochloride and the filtrate is concentrated in vacuo to give a brownish oil. Trituration of the crude oil with 200 mL of acetonitrile gives 36.65 g (85% yield) of a white solid: m.p.=195°-205° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292785
출처 데이터셋uspto-grants-1994_03
ORD IDord-28a6dfbc7a7345e7821328838a35d828
출처 메모uspto-grants-1994_03