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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2176732생성일: 2026년 10월 26일

Nordihydroguaretic acid → 1,4-bis{3,4-bis(2-methyl-thiazol-4-yl-methoxy)phenyl}-2,3-dimethyl-(2R,3S)-butane

https://huagongshe.com/reaction/2176732

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참여 물질

역할이름HCID투입량
반응물Nordihydroguaretic acidHCID 4534—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물4-(Chloromethyl)-2-methyl-1,3-thiazoleHCID 736341—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물1,4-bis{3,4-bis(2-methyl-thiazol-4-yl-methoxy)phenyl}-2,3-dimethyl-(2R,3S)-butaneHCID 5915987542.09%

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온도0 °C

반응 단계

To an ice-cooled solution of NDGA (1.50 g, 4.96 mol) in DMF (50 mL) was added 60% suspension of sodium hydride in paraffin (1.98 g=1.19 g NaH, 49.6 mmol, 10 mole equiv.). The mixture was stirred at 0° C. for 30 min. and at room temperature for 30 min. Then a solution of 4-chloromethyl-2-methylthiazole (5.86 g, 39.69 mmol, 8.0 mole equiv.) in DMF (20 mL) was added and the reaction mixture was allowed to stir for 16 h at room temperature. The reaction mixture was added to the saturated aqueous ammonium chloride (300 mL) and ether (600 mL). After shaking, the organic layer was separated, and the aqueous layer was extracted with ether (2×200 mL). The combined organic layer and extracts were washed with water (100 mL), brine (100 mL), and dried over anhydrous sodium sulfate and concentrated to dryness under reduced vacuum (30-40 mm Hg) at 25° C. The residue was dissolved in a minimum amount of dichloromethane and purified by silica gel flash chromatographic column using hexane:ethyl acetate (50:50 to 0:100) as eluant to give expected product as white solid (1.56 g, 42.09% yield). It was further purified by crystallization from acetate-hexane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09067875B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-d07ff72daf5a4ff19483043f85284492
출처 메모uspto-grants-2015_06