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HRID 1845720作成日:2026年10月27日

Ammonium Hydroxide → N-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethyl)-3-(tritylthio)propanamide

https://huagongshe.com/reaction/1845720

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Ethanol, 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]-HCID 160103—
反応物2,5-Dioxopyrrolidin-1-yl 3-(tritylthio)propanoateHCID 17935426—
溶媒DichloromethaneHCID 6344—
生成物N-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethyl)-3-(tritylthio)propanamideHCID 6892799682.7%

反応手順

Succinimido 3-(triphenylmethylthio)propanoate (4.06 mg, 9.12 mmol) was added to a 0° C. solution of 2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethanol (C. Bertozzi and M. Bednarski, J. Org. Chem. 1991, 56, 4326-4329) (9.12 mmol) in dichloromethane (20 mL). The solution was stirred at room temperature for 2 days and concentrated ammonium hydroxide (1 mL) was added. After 20 minutes, the mixture was filtered and the filtrate was subjected to an extractive workup. The organic layer were dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by HPFC on silica gel (gradient elution with 2-19% CMA in chloroform) to provide 3.95 g of N-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethyl)-3-(tritylthio)propanamide as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08951528B2
出典データセットuspto-grants-2015_02
ORD IDord-2dd8f0e9717841589cc67d31e5e128d2
出典メモuspto-grants-2015_02