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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285689Generated: October 25, 2026

Sodium hydride → 5-L-glutamyl-taurine

https://huagongshe.com/reaction/2285689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantSodium bromoethanesulfonateHCID 23705444—
Reactantcarbobenzyloxy-L-glutamine sodium saltHCID 70546861—
SolventDimethylformamideHCID 6228—
Product5-L-glutamyl-taurineHCID 68759—

Reaction Steps

3.02 g. (10 mmoles) of carbobenzyloxy-L-glutamine sodium salt (Liebig's Ann. 640, 145 /1961/) are dissolved in 50 ml. of dimethyl formamide, 12 mmoles of sodium hydride are added in the form of an oily dispersion, and the mixture is heated for 2 hours under exclusion of air humidity. Thereafter a solution of 2.11 g. (10 mmoles) of sodium bromoethanesulfonate in 50 ml. of dimethyl formamide is added dropwise, and the mixture is heated for additional 2 hours. The mixture is evaporated in vacuo. The residue is extracted with ether, then the dry substance is dissolved in water, and the solution is passed through a column filled with Dowex 50 ion exchanger. The column is eluted with water. The eluate is evaporated in vacuo, and the residue is dried over solid potassium hydroxide. The obtained substance is subjected to catalytic hydrogenation as described in Example 5. The product is recrystallized from a mixture of ethanol and water. 1.55 g. of gamma-L-glutamyl-taurine are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04324743
Source datasetuspto-grants-1982_04
ORD IDord-da5cbcf82c7e412ea838dd7772afafaf
Source noteuspto-grants-1982_04