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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854242생성일: 2026년 10월 27일

Tributylphosphine → 6-(3-Piperidin-1-yl-propoxy)-naphthalene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/854242

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물Piperidine-1-propanolHCID 66032—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물Methyl 6-hydroxy-2-naphthoateHCID 390995—
용매TetrahydrofuranHCID 8028—
생성물6-(3-Piperidin-1-yl-propoxy)-naphthalene-2-carboxylic acid methyl esterHCID 5893389376.4%

반응 단계

A mixture of 20.2 g (0.1 mol) 6-hydroxy-naphthalene-2-carboxylic acid methyl ester (commercially available), 18.6 g (0.13 mol) 1-piperidinepropanol (commercially available), 50.4 g (0.2 mol) 1,1′-(azodicarbonyl)dipiperidine and 58 ml (0.2 mol) tri-n-butyl-phosphine in 400 ml THF was stirred at room temperature for 16 h. The suspension was filtered off and the filtrate evaoprated to dryness. The residue was taken up in 200 ml DCM and 400 g Isolute® HM-N (Argonaut Technologies Inc., support material for accelerated solvent extraction) was added and evaporated to dryness. The residue was chromatographed over silica eluting with a gradient formed from DCM/MeOH(2N NH3) 99/1 to 9/1. After evaporation the residue was treated with heptan/diethyl ether and the precipitate filtered of and washed again with heptan/diethyl ether. After drying under reduced pressure at 50° C. 25 g (76%) of the title compound was obtained as white solid. MS (m/e): 328.3 (MH+, 100%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259158B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-02f4c9ea89154cd09ef829f9f0a3a884
출처 메모uspto-grants-2007_08