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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248562Generated: October 26, 2026

5-Aminovaleric acid → 5-(4-Dimethylaminobenzenesulphonylamino)valeric acid

https://huagongshe.com/reaction/2248562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminovaleric acidHCID 138—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant4-(Dimethylamino)benzene-1-sulfonyl chlorideHCID 12506943—
SolventWaterHCID 962—
Product5-(4-Dimethylaminobenzenesulphonylamino)valeric acidHCID 1172234061.7%

Reaction Steps

4.4 g of 4-dimethylaminobenzenesulphonyl chloride (Chem. Ber. 43, 3038, (1910)) are added to a solution comprising 2.34 g of 5-aminovaleric acid and 2.4 g of sodium hydroxide dissolved in 24 cm3 of water, followed by the addition of 24 cm3 of tetrahydrofuran in order to obtain a solution. The temperature rises to 36° C. The mixture is kept stirring for 4 hours, the tetrahydrofuran is evaporated off, the reaction medium is acidified using acetic acid and extracted with chloroform, the organic phase is dried and the solvents are removed under reduced pressure. 3.7 g of expected product are obtained. M.p. 105°-110° C. After crystallization in an isopropanol/water mixture (1:1), the product, melting point 118°-120° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041436
Source datasetuspto-grants-1991_08
ORD IDord-7b7cea8af58a4877bb955a8a5c20c01d
Source noteuspto-grants-1991_08