HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 2-[(6-chloronaphthalen-2-ylsulfonyl)amino]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Reactant | 6-Chloronaphthalene-2-sulfonyl chloride | HCID 10635129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-[(6-chloronaphthalen-2-ylsulfonyl)amino]acetate | HCID 23250750 | 101.4% |
Reaction Steps
Glycine ethyl ester hydrochloride (9.88 g) was suspended in methylene chloride (500 ml), and triethylamine (20.2 ml) and then 6-chloronaphthalene-2-sulfonyl chloride (17.6 g) were added to the suspension under cooling with ice. After stirring at room temperature for 1 hour and adjusting the mixture to pH 2 by addition of 1N hydrochloric acid, the mixture was extracted with methylene chloride. The methylene chloride layer was washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. After washing the resulting crystals in n-hexane, the crystals were collected by filtration and air-dried to obtain the title compound (22.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858599B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-b5bd6018b5cd40e6af74684320baea73 |
| Source note | uspto-grants-2005_02 |