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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1168634생성일: 2026년 10월 26일

Ethyl phosphorochloridite → Diethyl 2-[di(1-naphthyl)phosphino]phenylphosphonite

https://huagongshe.com/reaction/1168634

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl phosphorochloriditeHCID 68530—
반응물(2-Bromophenyl)[di(1-naphthyl)]phosphineHCID 11201532—
반응물ButyllithiumHCID 178418339—
생성물Diethyl 2-[di(1-naphthyl)phosphino]phenylphosphoniteHCID 11488538—

반응 단계

For example, 2-bromophenol (4) is reacted with trifluoromethanesulfonic anhydride to form 2-(trifluoromethanesulfonyl)oxy-bromobenzene (5), which is then reacted with di(1-naphthyl)phosphine in the presence of a palladium complex catalyst to obtain (2-bromophenyl)[di(1-naphthyl)]phosphine (6). Next, the compound (6) is reacted with diethyl chlorophosphite in the presence of n-butyllithium to obtain diethyl 2-[di(1-naphthyl)phosphino]phenylphosphonite (7). Then, the compound (7) is reduced with lithium aluminum hydride in the presence of chlorotrimethylsilane to form [2-[di(1-naphthyl)phosphino]phenylphosphine (8). Thereafter, in the presence of n-butyllithium, the compound is reacted with dimesylate of (2R,5R)-2,5-hexanediol producible, for example, according to the method described in a literature (Tetrahedron: Asymmetry, 1991, 2, 569), whereby the aimed (S,S)-Me-UCAP-(1-Nap) (3) can be produced in a high efficiency.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06624320B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-8d84efb14c304e389dcbe1ceaae42046
출처 메모uspto-grants-2003_09