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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295168Generated: October 26, 2026

Water → O-acetyl thyroxine

https://huagongshe.com/reaction/2295168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThyroxineHCID 5819—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductO-acetyl thyroxineHCID 86748204115.5%

Reaction Steps

The N-FMOC protected L-Thyroxine (26.3 g, 23.2 mmol) was dissolved in 150 mL THF, 3.28 mL (34.8 mmol) of acetic arthydride added, 283 mg (2.32 mmol) of 4-dimethylaminopyridine added, and reaction stirred under N2 for 45 minutes, then poured into 400 mL H2O and extracted with CHCl3 (3×400 mL). The CHCl3 extracts were combined, dried over Na2SO4, and solvent removed in vacuo. The residue was then purified by silica gel column chromatography, eluting with CH2 Cl2/MeOH/HOAc (90/10/0.4, v/v), to yield 21.95 g (91%) of the desired O-acetyl thyroxine as a beige solid; 1H NMR (300 MHz, DMSO-D6) d 7.12-7.91 (m, 12H), 4.07-4.31 (m, 4H), 3.07-3.19 (m, 1H), 2.82 (t, 1H), 2.29-2.40 (m, 3H); mass spec (FAB) (M+H)+1042.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691456
Source datasetuspto-grants-1997_11
ORD IDord-7d5878cb21b24565856514495de72b68
Source noteuspto-grants-1997_11