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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238627생성일: 2026년 10월 26일

Fluoresone → 4-(4-Ethanesulfonyl-phenoxy)-6-fluoro-3-methyl-naphthalene-2-carbaldehyde

https://huagongshe.com/reaction/238627

반응식

참여 물질

역할이름HCID투입량
반응물FluoresoneHCID 71814—
반응물HCID 59326572HCID 59326572—
생성물4-(4-Ethanesulfonyl-phenoxy)-6-fluoro-3-methyl-naphthalene-2-carbaldehydeHCID 59326523—

반응 단계

Starting with 6-fluoro-4-hydroxy-3-methyl-naphthalene-2-carbaldehyde (115 mg, 0.6 mmol) and 1-ethanesulfonyl-4-fluoro-benzene (226 mg, 1.2 mmol), using a method analogous to the one described for the methyl ester of example 1-1,4-(4-ethanesulfonyl-phenoxy)-6-fluoro-3-methyl-naphthalene-2-carbaldehyde (120 mg, 57%) was obtained as a yellow solid which was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ ppm 10.35 (s, 1H), 8.32 (s, 1H), 8.07 (dd, J=8.97, 5.68 Hz, 1H), 7.84 (d, J=9.09 Hz, 2H), 7.33-7.45 (m, 2H), 6.94 (d, J=8.84 Hz, 2H), 3.12 (q, J=7.41 Hz, 2H), 2.59 (s, 3H), 1.31 (t, J=7.45 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642629B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-752a5a4c67414063a250aeb2ed1829e4
출처 메모uspto-grants-2014_02