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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921109생성일: 2026년 10월 26일

Triphenylphosphine → Methyl 5-fluoro-2-(pent-4-en-2-yloxy)benzoate

https://huagongshe.com/reaction/921109

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Methyl 5-fluoro-2-hydroxybenzoateHCID 2783186—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물(2R)-pent-4-en-2-olHCID 6999724—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Methyl 5-fluoro-2-(pent-4-en-2-yloxy)benzoateHCID 11830705281%

반응 단계

To a solution of methyl 5-fluoro-2-hydroxybenzoate (1.0 g, 5.88 mmol), (R)-(−)-pent-4-en-2-ol (1.210 ml, 11.76 mmol) and triphenylphosphine (2.004 g, 7.64 mmol) in THF (14 ml) was added dropwise DIAD (1.486 ml, 7.64 mmol) and the resulting solution was stirred at rt. After 20 h, the reaction was diluted with Et2O and washed with 1N NaOH, water (3×'s) and brine. The organic phase was dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography (Biotage; 0%-40% EtOAc/hexane; 20 CV) to give methyl 5-fluoro-2-(pent-4-en-2-yloxy)benzoate (1.1331 g, 4.76 mmol, 81% yield) as a yellow oil. 1H NMR (400 MHz, CDCl3) δ 7.49 (dd, J=8.7, 3.3 Hz, 1H), 7.15 (ddd, J=8.9, 7.7, 3.4 Hz, 1H), 6.96 (dd, J=9.0, 4.2 Hz, 1H), 6.02-5.79 (m, 1H), 5.20-5.06 (m, 2H), 4.50-4.34 (m, 1H), 3.90 (s, 3H), 2.60-2.32 (m, 2H), 1.34 (d, J=6.1 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273067B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-ea84e7e8c279414b964ae8ccbd240ced
출처 메모uspto-grants-2016_03