HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556299Generated: October 25, 2026
Ethanesulfonyl chloride → 8-(Ethylsulfonylamino)octanoic acid
https://huagongshe.com/reaction/556299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | 8-Aminooctanoic acid | HCID 66085 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 8-(Ethylsulfonylamino)octanoic acid | HCID 21103229 | 38% |
Reaction Steps
A solution of ethanesulfonyl chloride (1.5 ml, 15.7 mmol) in dioxane (5 ml) was added to a solution of 8-aminooctanoic acid (1 g, 6.28 mmol) in 1N NaOH (22 ml) and dioxane (5 ml), while stirring at 0° C.-5° C. The mixture was allowed to warm to room temperature and stirred for 3.5 minutes. During this period, at 1 hour intervals, the pH was adjusted to 7-8 by addition of 25% NaOH solution. The reaction mixture was washed with diethyl ether (30 ml). The pH was adjusted to 1-2 by addition of 1N HCl and the mixture was extracted with ethyl acetate (70 ml). The organic layer was dried over sodium sulfate and concentrated. The residue was triturated with a mixture of diethyl ether. The solid was collected by filtration and dried under vacuum affording 600 mg of the title compound (38% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08058262B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-61306cc242ae4b8896c94c35ab722da1 |
|---|
| Source note | uspto-grants-2011_11 |
|---|