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HRID 1292348作成日:2026年10月25日

Lithium Hydroxide → 2-(4-(1-(Tert-butoxycarbonyl)piperidin-4-yloxy)-2-methoxyphenyl)acetic acid

https://huagongshe.com/reaction/1292348

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium HydroxideHCID 3939—
反応物Methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)phenylacetateHCID 18914175—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-(1-(Tert-butoxycarbonyl)piperidin-4-yloxy)-2-methoxyphenyl)acetic acidHCID 18914169—

反応手順

Methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)phenylacetate (1.37 g, 3.6 mmol) was dissolved in THF (27 ml) and treated with lithium hydroxide (4.5 ml of a 1M aqueous solution, 4.5 mmol). The mixture was stirred at ambient temperature for 4.5 hours, then treated with an additional 0.9 ml of 1M lithium hydroxide and stirred at ambient temperature for 18 hours. The mixture was concentrated in vacuo, and the residue was acidified with 1M HCl, and extracted with ethyl acetate. The combined ethyl acetate layers were dried over sodium sulfate, filtered, and evaporated to dryness in vacuo. The residue was reconcentrated from ether to give 2-methoxy-4-(1-Boc-4-piperidyloxy)phenylacetic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05756504
出典データセットuspto-grants-1998_05
ORD IDord-f18b6242e2da413b9f697b4d24450bb6
出典メモuspto-grants-1998_05