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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732551Generated: October 26, 2026

Sodium Chloride → N-Trifluoroacetylthyroxine

https://huagongshe.com/reaction/1732551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantThyroxineHCID 5819—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-TrifluoroacetylthyroxineHCID 12831641—

Reaction Steps

A solution of 20 g [25.6 millimoles (mmol)] of L-thyroxine (Sigma Chemical Co., St. Louis, Missouri USA) in 240 ml of dry ethyl acetate containing 46 ml of trifluoroacetic acid and 7.6 ml of trifluoroacetic anhydride was stirred at 0° C. for one hour. Upon warming to room temperature and adding 200 ml of H2O, a suspension formed which was then saturated with sodium chloride. The organic phase of the mixture was separated, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated to give 21.3 g of the N-protected thyroxine derivative (6). A sample was recrystallized from ether-pentane to give fine crystals, m.p. 233°-235° C. (decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238395
Source datasetuspto-grants-1980_12
ORD IDord-1e1e0100439043f4b027b084bc7361ed
Source noteuspto-grants-1980_12