HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → Methyl 4-(2-p-toluenesulphonamido-indan-5-yl)-4-oxobutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-(2-amino-indan-5-yl)-4-oxobutyrate hydrochloride | HCID 23050575 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 4-(2-p-toluenesulphonamido-indan-5-yl)-4-oxobutyrate | HCID 14071511 | — |
Reaction Steps
6.0 g (21.1 mmol) of methyl 4-(2-amino-indan-5-yl)-4-oxobutyrate hydrochloride are suspended in 60 ml of chloroform and 5.0 g (25.3 mmol) of p-toluenesulphonyl chloride are added. 5.1 g (50 mmol) of triethylamine are added, with vigorous stirring, a clear solution being formed. After 20 hours at room temperature, the mixture is washed with water, the chloroform solution is evaporated and the residue is recrystallised from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04820705 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-108a7eafbf084c76b4f02daf629fd8bc |
| Source note | uspto-grants-1989_04 |