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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420124Generated: October 31, 2026

Hexanoyl chloride → HCID 86754010, compound

https://huagongshe.com/reaction/1420124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexanoyl chlorideHCID 67340—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 118007HCID 118007—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86754010HCID 86754010—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 1 equiv. 3,3'-dithiobis(2-aminopropionic acid) dimethylester dihydrochloride in tetrahydrofuran (white slurry) was stirred and cooled to 0° C. To the reaction mixture was added 4 equiv. of N-ethyldiiso-propylamine and 2.2 equiv. of hexanoylchloride. The mixture was stirred for 4 hrs on an ice bath and the white precipitate of N-ethyldiisopropylammonium chloride was filtered off. The solvent was removed by evaporation under reduced pressure and the crude product was redissolved in dichlormethane. After washing with water, the organic phase was dried over sodium sulphate. Filtration and evaporation of the solvent gave crude (R,R)-N,N'-dihexanoyl-3,3'-dithiobis(2-aminopropionic acid) dimethylester, which was recrystallized from methanol/water and triturated with diethylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889050
Source datasetuspto-grants-1999_03
ORD IDord-481e5dfe43ed4ef7a25e114ea048e016
Source noteuspto-grants-1999_03