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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295167Generated: October 26, 2026

Hydrochloric Acid → N-Acetylthyroxine

https://huagongshe.com/reaction/2295167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
ReactantLevothyroxine SodiumHCID 23666112—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventSodium HydroxideHCID 14798—
ProductN-AcetylthyroxineHCID 2063838090%

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691456
Source datasetuspto-grants-1997_11
ORD IDord-099d6b2550044c45b1f2a3cd5cf09785
Source noteuspto-grants-1997_11