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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129792생성일: 2026년 10월 24일

Triphenylphosphine → HCID 19705817, 화합물

https://huagongshe.com/ko/reaction/129792

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-PropylphenolHCID 12580—
반응물6-Bromo-1-hexanolHCID 77970—
반응물Diisopropyl azodicarboxylateHCID 5363146—
용매TetrahydrofuranHCID 8028—
생성물HCID 19705817HCID 1970581767%

반응 단계

A solution of diisopropylazodicarboxylate (2.12 g, 10.5 mmol) in THF (25 mL) was added via syringe pump over 1.5 h to a mixture of 4-propylphenol (purchased from Aldrich Chemical Co.) (1.36 g, 10.0 mmol), 6-bromo-1-hexanol (purchased from Aldrich Chemical Co.) (1.81 g, 10.0 mmol), and triphenylphosphine (2.75 g, 10.5 mmol) in THF (25 mL) at 0° C. under argon. The slightly yellow reaction was stirred at 0° C. for 30 min, whereupon additional triphenylphosphine (262 mg, 1.00 mmol) was added, followed by addition of diisopropylazodicarboxylate (200 mL, 1.0 mmol) over 30 min. The reaction was allowed to warm to RT, at which time silica gel (15 g) was added. The mixture was concentrated in vacuo and the white powder obtained was purified by flash chromatography on silica gel (150 g) eluted with a step gradient of hexane to 2:98 EtOAc/hexane. The slightly impure product obtained was rechromatographed on silica gel (150 g) eluted with 1:99 EtOAc/hexane to give title compound (2.00 g, 67%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05470845
출처 데이터셋uspto-grants-1995_11
ORD IDord-7ec61da8bc61441bb34fb6ae35e507b0
출처 메모uspto-grants-1995_11