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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493369생성일: 2026년 10월 25일

Glycidyl benzoate → 2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate

https://huagongshe.com/reaction/493369

반응식

참여 물질

역할이름HCID투입량
반응물Glycidyl benzoateHCID 25998—
반응물N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanineHCID 14217229—
촉매Tetrabutylammonium BromideHCID 74236—
용매TolueneHCID 1140—
생성물2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoateHCID 6020725226%

반응 단계

A solution of oxiran-2-ylmethyl benzoate (3.0 g, 16.8 mmol), (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoic acid (6.0 g, 20.2 mmol), and tetrabutylammonium bromide (542 mg, 1.7 mmol) in anhydrous toluene was heated to 90° C. for 18 hrs. The reaction mixture was concentrated to dryness under reduced pressure, diluted with ethyl acetate, and washed with water twice followed by the addition of a saturated NaHCO3 solution and brine. The organic layer was dried through MgSO4 and concentrated under reduced pressure. Chromatography (silica gel, 1:1 ethyl acetate/hexane) of the residue afforded 2.05 g (26%) of 2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534813B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-103513a5c7d04c64a75856069b1bb3ae
출처 메모uspto-grants-2009_05