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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1011671생성일: 2026년 10월 25일

Triphenylphosphine → methyl 3-(benzyloxy)-5-{(1S)-1-methyl-2-[(triisopropylsilyl)oxy]ethoxy}benzoate

https://huagongshe.com/reaction/1011671

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물Methyl 3-(benzyloxy)-5-hydroxybenzoateHCID 7472028—
반응물(2R)-1-{[Tri(propan-2-yl)silyl]oxy}propan-2-olHCID 57504697—
용매TetrahydrofuranHCID 8028—
생성물methyl 3-(benzyloxy)-5-{(1S)-1-methyl-2-[(triisopropylsilyl)oxy]ethoxy}benzoateHCID 5362962271.4%

반응 조건

온도0 °C

반응 단계

(2R)-1-[(Triisopropylsilyl)oxy]propan-2-ol (56.1 g, 242 mmol) was added to a solution of methyl 3-hydroxy-5-{[phenylmethyl]oxy}benzoate (50 g, 194 mmol) and triphenylphosphine (63.5 g, 242 mmol) in dry THF (500 mL), at to 0° C., followed by addition of DIAD (47.6 mL, 242 mmol) over 45 minutes under an argon atmosphere. The reaction was stirred at 0° C. for 1 hour and allowed to warm up to RT over an hour then stirred at RT for 1 hour. The THF was evaporated and a mixture of ethyl acetate (80 mL) and hexane (120 mL) was added. This mixture stirred for 2 hours and filtered. The precipitate was washed with a mixture of ethyl acetate (20 mL) and hexane (180 mL) and the filtrate evaporated. The residue was purified by column chromatography, eluting with 1:20 to 1:10 ethyl acetate:hexanes, to afford the title compound (65.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07977328B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-74e98af1b9cc40f49151d41863342dad
출처 메모uspto-grants-2011_07