HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 11-(2-benzoyl-4-chlorobenzenesulphonamido)undecanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-benzoyl-4-chloro-benzenesulfonyl Chloride | HCID 2756600 | — |
| Reactant | Ethyl 11-aminoundecanoate hydrochloride | HCID 13192101 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 11-(2-benzoyl-4-chlorobenzenesulphonamido)undecanoate | HCID 22152233 | — |
Reaction Steps
7 ml of anhydrous triethylamine are added to 5.3 g of ethyl 11-aminoundecanoate hydrochloride in 30 ml of anhydrous methylene chloride and, after stirring for one hour at ambient temperature, 6.3 g of 2-benzoyl-4-chlorobenzenesulphonyl chloride are added dropwise. After stirring for 12 hours, the reaction medium is evaporated to dryness under vacuum, taken up with water and extracted with ethyl acetate. The organic phase which is washed with water until the washings are free of Cl- ions is dried over sodium sulphate and evaporated to dryness under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980349 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-0e1e648f1e614fd5b802cf141116c059 |
| Source note | uspto-grants-1990_12 |