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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1386408생성일: 2026년 10월 26일

Triphenylphosphine → 6-[2-(1H-1-imidazolyl)ethoxy]-7-methyl-1,2,3,4-tetrahydro-1-naphthalenone

https://huagongshe.com/reaction/1386408

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물N-(2-Hydroxyethyl)imidazoleHCID 74168—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물6-Hydroxy-7-methyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 18626482—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물6-[2-(1H-1-imidazolyl)ethoxy]-7-methyl-1,2,3,4-tetrahydro-1-naphthalenoneHCID 1862650532.9%

반응 단계

Under N2, a solution of 2.08 g (11.8 mmol) of 6-hydroxy-7-methyl-1,2,3,4-tetrahydro-1-naphthalenone in 25 mL of THF was treated with 1.46 g (13.9 mmol) of 2-(1H-1-imidazolyl)-1-ethanol and 3.1 g (11.8 mmol) of triphenylphosphine. The solution was cooled in ice and treated with a solution of 1.9 mL (11.8 mmol) of diethyl azodicarboxylate in 5 mL of THF. The solution was allowed to stir at room temperature overnight. The mixture was diluted with EtOAc and washed twice with H2O, twice with saturated NaHCO3, then with saturated NaCl. Drying over MgSO4 and removal of the solvent under pressure left the crude product. Chromatography on silica gel, eluting with CHCl3/MeOH (95/5) gave the product which was recrystallized from EtOAc/hexane to give 1.05 g (32.9% yield) of the product as a tan solid, mp 118-120° C. The structure was confirmed by NMR and mass spectroscopy. MS m/z 271 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06265422B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-664c59cbb62b48df94741240e6f2dcbb
출처 메모uspto-grants-2001_07