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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921218생성일: 2026년 10월 26일

Triphenylphosphine → (S)-methyl 1-(pent-4-en-2-yloxy)-2-naphthoate

https://huagongshe.com/reaction/921218

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2-Naphthalenecarboxylic acid, 1-hydroxy-, methyl esterHCID 70358—
반응물Diethyl azodicarboxylate, (Z)-HCID 5354216—
반응물(2R)-pent-4-en-2-olHCID 6999724—
용매TetrahydrofuranHCID 8028—
생성물(S)-methyl 1-(pent-4-en-2-yloxy)-2-naphthoateHCID 11830716074.8%

반응 단계

A mixture of methyl 1-hydroxy-2-naphthoate (500 mg, 2.473 mmol), (R)-pent-4-en-2-ol (0.382 mL, 3.71 mmol), triphenylphosphine (1297 mg, 4.95 mmol) and (Z)-diethyl diazene-1,2-dicarboxylate (0.836 mL, 4.95 mmol) in THF (20 mL) was stirred at rt for 3 h. It was then concentrated and the residue was purified by biotage, eluting with 10% EtOAc/hexane to isolate (S)-methyl 1-(pent-4-en-2-yloxy)-2-naphthoate (500 mg, 74.8%) as an oil. 1H NMR (400 MHz, CDCl3) δ 8.41-8.27 (m, 1H), 7.96-7.81 (m, 2H), 7.69-7.45 (m, 3H), 5.89 (ddt, J=17.2, 10.1, 7.1 Hz, 1H), 5.22-5.04 (m, 2H), 4.49-4.29 (m, 1H), 3.99 (s, 3H), 2.66-2.57 (m, 1H), 2.55-2.46 (m, 1H), 1.28 (d, J=6.4 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273067B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-2f9c33b311b1474ba6ffe53a4c34d604
출처 메모uspto-grants-2016_03