HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Aminovaleric acid → 5-(4-Dimethylaminobenzenesulphonylamino)valeric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Aminovaleric acid | HCID 138 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Dimethylamino)benzene-1-sulfonyl chloride | HCID 12506943 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(4-Dimethylaminobenzenesulphonylamino)valeric acid | HCID 11722340 | 61.7% |
Reaction Steps
4.4 g of 4-dimethylaminobenzenesulphonyl chloride (Chem. Ber. 43, 3038, (1910)) are added to a solution comprising 2.34 g of 5-aminovaleric acid and 2.4 g of sodium hydroxide dissolved in 24 cm3 of water, followed by the addition of 24 cm3 of tetrahydrofuran in order to obtain a solution. The temperature rises to 36° C. The mixture is kept stirring for 4 hours, the tetrahydrofuran is evaporated off, the reaction medium is acidified using acetic acid and extracted with chloroform, the organic phase is dried and the solvents are removed under reduced pressure. 3.7 g of expected product are obtained. M.p. 105°-110° C. After crystallization in an isopropanol/water mixture (1:1), the product, melting point 118°-120° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041436 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-7b7cea8af58a4877bb955a8a5c20c01d |
| Source note | uspto-grants-1991_08 |