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HRID 1107174생성일: 2026년 10월 25일

Benzoic Acid → (E)-2-t-Butoxycarbonyl-7-phenylhept-2-enyl benzoate

https://huagongshe.com/reaction/1107174

반응식

참여 물질

역할이름HCID투입량
반응물Benzoic AcidHCID 243—
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물t-Butyl 2-(1-hydroxy-5-phenylpentyl)acrylateHCID 18790144—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물(E)-2-t-Butoxycarbonyl-7-phenylhept-2-enyl benzoateHCID 6990794082%

반응 조건

온도0 °C

반응 단계

Diisopropyl azodicarboxylate (5 mL, 25 mmol) is added dropwise over 5 minutes to a solution of t-butyl 2-(1-hydroxy-5-phenylpentyl)acrylate (5.59 g, 19.3 mmol), benzoic acid (3 g, 25 mmol) and triphenyl phosphine (6.5 g, 25 mmol) in THF (100 mL) at -55° C. The reaction is maintained between -55 and -50° C. for 45 minutes and then the reaction is allowed to warm to 0° C. The solution is diluted with ether (300 mL) and washed with 1 N NaOH (2×40 mL) and brine (70 mL). The resulting solution is dried (MgSO4) and concentrated in vacuo. The crude reaction product is partially dissolved in 20% ether/petroleum ether and applied to a silica gel column as a slurry. The column is eluted using gradient elution (silica, 10 to 20% ether in petroleum ether) to obtain (E)-2-t-Butoxycarbonyl-7-phenylhept-2-enyl benzoate (6.2 g, 82%): 1H NMR (300 MHz, CDCl3) δ 8.01 (d, J=7.0 Hz, 2H), 7.53-7.49 (m, 1 H), 7.41 (t, J=7.5 Hz, 2H), 7.28-7.23 (m, 2H), 7.20-7.10 (m, 3H), 6.99 (t, J=7.8 Hz, 1H), 5.05 (s, 2H), 2.61 (t, J=7.5 Hz, 2H), 2.36 (q, J=7.5 Hz, 2H), 1.72-1.46 (m, 4H), 1.47 (s, 9H); MS (FAB) m/e 395 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06057369
출처 데이터셋uspto-grants-2000_05
ORD IDord-1ebdc7453fe34652a7f7d213f1401545
출처 메모uspto-grants-2000_05