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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279820Generated: October 26, 2026

Water → t-Butoxycarbonylglycyl thyroxine methyl ester

https://huagongshe.com/reaction/279820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantN-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
ReactantMethyl O-(4-hydroxy-3,5-diiodophenyl)-3,5-diiodo-L-tyrosinateHCID 13911218—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
Productt-Butoxycarbonylglycyl thyroxine methyl esterHCID 18602701—

Reaction Steps

To the aforesaid Boc-Gly-OSu solution the thyroxine methyl ester solution was added while ice cooling. After permitting the same to warm to room temperature, the mixture was stirred for 1.5 hr. After letting the reaction mixture stand overnight, 25 ml. of distilled water and 50 ml. of ethyl acetate were added thereto and the mixture was extracted with ethyl acetate. The extraction was repeated three times using 25 ml. of ethyl acetate. The ethyl acetate layers were combined and dried over anhydrous magnesium sulfate. The liquid was concentrated using a rotary evaporator and subjected to gel chromatography using a column filled with Sephadex LH-20 (made by Pharmacia Co., Ltd.). As the solvent, a mixture obtained by mixing acetone and methanol in a proportion of 4:1 (volume) was used. While confirming by TLC, the objective fraction was taken and concentrated under reduced pressure followed by crystallization. The product was obtained in an amount of 950 mg. (yield 82.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04587102
Source datasetuspto-grants-1986_05
ORD IDord-7ec2364d73ff4c30b447b924255c2d63
Source noteuspto-grants-1986_05