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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265310생성일: 2026년 10월 26일

3-(Dimethylamino)phenol → 6-[[3-(N,N-dimethylamino)-phenyloxy]methyl]-1,2-dithiin

https://huagongshe.com/reaction/265310

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참여 물질

역할이름HCID투입량
반응물3-(Dimethylamino)phenolHCID 7421—
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물3-[(Tert-butyldimethylsilyloxy)methyl]-6-hydroxymethyl-1,2-dithiinHCID 10062832—
용매TetrahydrofuranHCID 8028—
생성물6-[[3-(N,N-dimethylamino)-phenyloxy]methyl]-1,2-dithiinHCID 8675106963%

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온도0 °C

반응 단계

To a stirred solution of 200 mg (0.688 mmol) of 3-(hydroxymethyl)-6-[(tert-butyldimethylsilyloxy)methyl]-1,2-dithiin (U.S. Ser. No. 08/212,096) in 2 mL dry THF was added a solution of 3--N,N-dimethylaminophenol (190 mg, 1.376 mmol) in 2 mL THF, followed by addition of (220 mg, 0.839 mmol) triphenylphosphine. The resulting solution was cooled to 0° C., then 140 μL (155 mg, 0.890 mmol) of diethylazodicarboxylate was added, and the reaction mixture was kept at 0°-5° C. for 3 h until TLC analysis showed the reaction to be complete. For isolation of the products the reaction mixture was chromatographed directly on silica gel column, using ethyl acetate-hexane, 1:3 to yield 3-[tert-butyldimethylsilyloxy)methyl]-6-[[3-(N,N-dimethylamino)-phenyloxy]methyl]-1,2-dithiin (115 mg, 41.1%); 1H-NMR (CDCl3) δ7.3 (bs, 1 H), 7.1 (bs, 1 H), 6.60 (d, J=2.4, 1 H), 6.52 (bd, J=7.27 1 H), 6.42 (d, J=6.0, 1 H), 6.34 (d, J=6.0, 1 H), 4.60 (s, 2 H), 4.26 (s, 2 H), 2.65 (s, 6 H), 0.88 (s, 9 H), 0.07 (s, 6 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648354
출처 데이터셋uspto-grants-1997_07
ORD IDord-0abb10cc76074099818aab159509c646
출처 메모uspto-grants-1997_07