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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1534384생성일: 2026년 10월 27일

Triphenylphosphine → 1-Methoxypropylthiazole

https://huagongshe.com/reaction/1534384

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물HydroxypropyleneHCID 143500—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물2-Propen-1-ol, 3-(3-pyridinyl)-HCID 3563504—
반응물3-[1-Methoxy-1-(1,3-thiazol-2-yl)propyl]phenolHCID 15637379—
용매TetrahydrofuranHCID 8028—
생성물1-MethoxypropylthiazoleHCID 2161875469.4%

반응 단계

Diethyl azodicarboxylate (0.38 ml) was added dropwise to a mixture of 2-[1-(3 hydroxyphenyl)-1-methoxypropyl]thiazole (0.37 g), triphenylphosphine (0.57 g), 3-(3-pyridyl)prop-2-en-1-ol (0.27 g) and tetrahydrofuran (7 ml) which had been cooled to 0°-5° C. in an ice-bath. The mixture was stirred at this temperature range for 2 hours and then at ambient temperature for 4 hours. Further portions of diethyl azodicarboxylate (0.1 ml), triphenylphosphine (0.14 g) and the propenol (0.045 g) were added and the mixture was stirred at ambient temperature for 18 hours. The mixture was partitioned between ethyl acetate (40 ml) and dilute aqueous hydrochloric acid (40 ml). The aqueous layer was separated and basified by adding potassium carbonate portionwise. The resulting solution was extracted with ethyl acetate (3×20 ml). The combined extracts were dried (Na2SO4) and evaporated. The residue was purified by column chromatography eluting with toluene/ethyl acetate (2/3 v/v) to give 2-[1-[3-(3-pyridyl)prop-2-en-1-yloxy)phenyl[-1-methoxypropylthiazole as a colourless oil (0.162 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05089495
출처 데이터셋uspto-grants-1992_02
ORD IDord-d942e4864a154653a4c59578476f70e2
출처 메모uspto-grants-1992_02