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HRID 1436729생성일: 2026년 10월 25일

Potassium Fluoride → (2S,3S)-2-dibenzylamino-4-nitro-1-phenyloct-7-en-3-ol

https://huagongshe.com/reaction/1436729

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물5-Nitropent-1-eneHCID 534297—
반응물(alphaS)-alpha-[Bis(phenylmethyl)amino]benzenepropanalHCID 9883943—
반응물4-[[1-(Anthracen-9-ylmethyl)-5-ethenyl-1-azoniabicyclo[2.2.2]octan-2-yl]-prop-2-enoxymethyl]quinoline;bromideHCID 22324578—
용매TetrahydrofuranHCID 8028—
생성물(2S,3S)-2-dibenzylamino-4-nitro-1-phenyloct-7-en-3-olHCID 69018478—

반응 조건

온도-10 °C

반응 단계

Cool to −10° C. a well stirred mixture of O-allyl-N-(9-anthracenylmethyl)-cinchonidinium bromide (0.480 g, 0.8 mmol), potassium fluoride (3 gr, 51 mmol), THF (150 mL) and 5-nitropent-1-ene (2.34 g, 20 mmol) and treat with a solution of (S)-2-dibenzylamino-3-phenylpropionaldehyde (2.640 gr, 8 mmol). Allow mixture to warn to room temperature and stir for two days. Concentrate under reduced pressure. Purify on silica gel with hexane/ethyl ether mixtures to give a mixture of two products (2.7 g, 75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618978B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-a6fd4c4b937841c494c7c56abd2d9158
출처 메모uspto-grants-2009_11