Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 118007 | HCID 118007 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86754010 | HCID 86754010 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05889050 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-481e5dfe43ed4ef7a25e114ea048e016 |
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| Source note | uspto-grants-1999_03 |
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