HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253400Generated: October 25, 2026
Methanesulfonic Acid → di[6-(N,N-diethyl)aminohexyl]3,3'-dithiodipropionate
https://huagongshe.com/reaction/1253400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 3,3'-Dithiodipropionic acid | HCID 95116 | — |
| Reactant | 6-(Diethylamino)-1-hexanol | HCID 245054 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | di[6-(N,N-diethyl)aminohexyl]3,3'-dithiodipropionate | HCID 59584812 | — |
Reaction Steps
1.3 g of methanesulfonic acid (manufactured by Wako Pure Chemical Industries, Ltd.) was added dropwise, under an atmosphere of nitrogen and at 70° C., to 2.3 g of the obtained 6-(N,N-diethyl)amino-1-hexanol. After stifling for 10 minutes, 1.4 g of 3,3′-dithiodipropionic acid (manufactured by Wako Pure Chemical Industries, Ltd.) was added, and the resulting mixture was heated to 120° C. and then stirred at 110° C. for 4 hours. Following completion of the reaction, the reaction mixture was cooled to room temperature and then added gradually to 50 mL of methyl isobutyl ketone (manufactured by Wako Pure Chemical Industries, Ltd.). After stirring for 2 hours, the precipitated crystals were collected by filtration and washed with acetone, yielding the methanesulfonate salt of di[6-(N,N-diethyl)aminohexyl]3,3′-dithiodipropionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08455413B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-8d6007077784428b8f31c7e3d6b9d121 |
|---|
| Source note | uspto-grants-2013_06 |
|---|