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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294509생성일: 2026년 10월 27일

Hydrochloric Acid → N-Acetylthyroxine

https://huagongshe.com/reaction/2294509

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acetic AnhydrideHCID 7918—
반응물Levothyroxine SodiumHCID 23666112—
용매EthanolHCID 702—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Sodium HydroxideHCID 14798—
용매Ammonium HydroxideHCID 14923—
생성물N-AcetylthyroxineHCID 2063838090%

반응 단계

L-Thyroxine sodium salt, pentahydrate (1) (10 g, 11 mmol) was nearly completely dissolved in 400 mL of ETCH/2 N 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 1.60 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05688921
출처 데이터셋uspto-grants-1997_11
ORD IDord-2ba69dc8a34244c79b3352a3a0e854b7
출처 메모uspto-grants-1997_11