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HRID 354299作成日:2026年10月26日

Triphenylphosphine → 4-[1-(Tert-butoxycarbonyl)-2-pyrrolidinyl]methoxy-1-iodo-3-methylbenzene

https://huagongshe.com/reaction/354299

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物4-Iodo-2-methylphenolHCID 143713—
反応物(S)-(-)-N-Boc-prolinolHCID 643448—
反応物Diisopropyl azodicarboxylateHCID 5363146—
溶媒TetrahydrofuranHCID 8028—
生成物4-[1-(Tert-butoxycarbonyl)-2-pyrrolidinyl]methoxy-1-iodo-3-methylbenzeneHCID 2351244778%

反応条件

温度70 °C

反応手順

To a stirred solution of 4-iodo-2-methylphenol (465 mg, 1.987 mmol), N-tert-butoxycarbonylprolinol (400 mg, 1.987 mmol), and Ph3P (625 mg, 2.384 mmol) in THF (7 mL) was added dropwise DIAD (0.5 mL, 2.404 mmol) at room temp, and the mixture was stirred for 13 hr at 70° C. The reaction mixture was concentrated in vacuo and the residue was chromatographed on silica-gel with n-hexane-EtOAc (9:1, v/v) as eluent to give 645.3 mg (78%) 4-[1-(tert-butoxycarbonyl)-2-pyrrolidinyl]methoxy-1-iodo-3-methylbenzene as a pale yellow oil. 1H-NMR (400 MHz, CDCl3) δ1.47 (s, 9H), 1.83-1.89 (m, 1H), 1.96-2.04 (m, 3H), 2.16 (s, 3H), 3.37-3.43 (br m, 2H), 3.81, 3.94 (br m each, 1H), 4.08-4.18 (m, 2H), 6.62 (br s, 1H), 7.42 (s, 2H); MS (FAB) m/z 418 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06756378B2
出典データセットuspto-grants-2004_06
ORD IDord-237852e4b0de4b2bba8c32fbe85e796c
出典メモuspto-grants-2004_06