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HRID 921218作成日:2026年10月26日

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

https://huagongshe.com/reaction/921218

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物2-Naphthalenecarboxylic acid, 1-hydroxy-, methyl esterHCID 70358—
反応物Diethyl azodicarboxylate, (Z)-HCID 5354216—
反応物(2R)-pent-4-en-2-olHCID 6999724—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-methyl 1-(pent-4-en-2-yloxy)-2-naphthoateHCID 11830716074.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09273067B2
出典データセットuspto-grants-2016_03
ORD IDord-2f9c33b311b1474ba6ffe53a4c34d604
出典メモuspto-grants-2016_03