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HRID 382766作成日:2026年10月25日

Sodium Iodide → (3-Azidopropyl)oxyacetic Acid

https://huagongshe.com/reaction/382766

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Sodium hydrideHCID 24758—
反応物3-Azidopropan-1-olHCID 10996974—
反応物Sodium chloroacetateHCID 23665759—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒TetrahydrofuranHCID 8028—
生成物(3-Azidopropyl)oxyacetic AcidHCID 2300413758%

反応手順

A solution of 3-azidopropanol (70.1 g, 0.693 mol) in 100 mL of THF was added dropwise, in a period of 1.5 hours, to a mechanically stirred suspension of NaH (60% in mineral oil, 30.5 g, 0.763 mol) in 250 mL of THF. During the addition of 3-azidopropanol, a gentle reflux was maintained. This was followed by addition of solid NaI (10.4 g, 69.3 mmol), and tetrabutylammonium bromide (22.3 g, 69.3 mmol), and sodium chloroacetate (88.8 g, 0.763 mol). The reaction mixture was heated at reflux temperature for 19 hours, cooled, quenched initially with 20 mL of water (added dropwise) and then with 700 mL of water, washed with EtOAc (3×200 mL), acidified with concentrated HCl to pH=2, and extracted with dichloromethane (6×100 mL). The combined dichloromethane extracts were dried (MgSO4), and the solvent was removed in vacuo to give 63.3 g (58%) of the title compound as a yellow viscous oil. The crude product was used in the next step after spectral characterization.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06310076B1
出典データセットuspto-grants-2001_10
ORD IDord-610556191b1140d3bac4834f993eeec7
出典メモuspto-grants-2001_10