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HRID 233427生成日期:2026年10月23日

海萝胶 → N-乙酰基L-甲状腺素

https://huagongshe.com/zh-CN/reaction/233427

反应方程式

参与物

角色名称HCID投料
反应物海萝胶HCID 313—
反应物乙酐HCID 7918—
反应物L-Thyroxine monosodium saltHCID 23666112—
溶剂乙醇HCID 702—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
溶剂N,N-二甲基甲酰胺HCID 6228—
溶剂二甲基对苯二胺二盐酸HCID 14798—
产物N-乙酰基L-甲状腺素HCID 2063838090%

反应步骤

L-Thyroxine sodium salt, pentahydrate (1) (10 g, 11 mmol) was nearly completely dissolved in 400 mL of EtOH/2N NH4OH (1/1, v/v), filtered, and filtrate poured into 425 mL of 5% HCl. The resulting precipitate was isolated by vacuum filtration and dried under high vacuum to afford a white solid. This material was dissolved in 160 mL DMF, 100 mL (1.06 mol) of acetic anhydride added, and reaction stirred for 1.5 hours, then diluted with 850 mL H2O and allowed to stand at 4° C. for 16 hours. The resulting precipitate was isolated by filtration, then dissolved in 350 mL EtOH and 41 mL of 1N NaOH, stirred for 2.5 hours, 680 mL of 5% HCl added, and mixture allowed to stand at 4° C. for 16 hours. The resulting precipitate was isolated by vacuum filtration and dried under high vacuum to yield 8.1 g (90%) of the desired N-acetyl L-thyroxine (5) as a white solid; 1H NMR (200 MHz, CD3OD) d 7.8 (s, 2H), 7.1 (s, 2H), 4.6-4.7 (m, 1H), 2.8-3.0 (m, 2H), 2.0 (s, 3H); mass spec (FAB) (M+H)+ 820.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05593896
来源数据集uspto-grants-1997_01
ORD IDord-97e385cdd7e44f0396ea95960748bd36
来源说明uspto-grants-1997_01