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HRID 350352作成日:2026年10月25日

Triphenylphosphine → dimethyl (S)-4-[1-(tert-butoxycarbonyl)-2-pyrrolidinylmethoxy]phthalate

https://huagongshe.com/reaction/350352

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Dimethyl 4-hydroxyphthalateHCID 89726—
反応物(S)-(-)-N-Boc-prolinolHCID 643448—
反応物Diisopropyl azodicarboxylateHCID 5363146—
溶媒TetrahydrofuranHCID 8028—
生成物dimethyl (S)-4-[1-(tert-butoxycarbonyl)-2-pyrrolidinylmethoxy]phthalateHCID 86587781102.5%

反応手順

To a stirred solution of dimethyl 4-hydroxyphthalate (3.00 g, 14.27 mmol), N-Boc-prolinol (2.87 g, 14.26 mmol), Ph3P (4.49 g, 17.12 mmol) in THF (50 mL) was added DIAD (3.40 mL, 17.27 mmol) at 0° C. Then the resulting mixture was heated under reflux overnight. The resulting mixture was evaporated and the residue was purified by column chromatography on silica-gel with n-hexane-EtOAc (3:1, v/v) as eluent to give 5.75 g (q.y.) dimethyl (S)-4-[1-(tert-butoxycarbonyl)-2-pyrrolidinyl methoxy]phthalate as an oil. 1H-NMR (CDCl3) δ 1.47 (s, 9 H), 1.86–2.05 (m, 4 H), 3.36–3.40 (m, 2 H), 3.87 (m, 3 H), 3.91 (s, 3 H), 3.96–4.19 (m, 3 H), 7.03–7.24 (m, 2 H), 7.80 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179819B2
出典データセットuspto-grants-2007_02
ORD IDord-380a6cafc6304821b828eb1d927d7463
出典メモuspto-grants-2007_02