HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Aminovaleric acid → HCID 10471725, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Aminovaleric acid | HCID 138 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Diethylamino)benzenesulfonyl chloride | HCID 19811005 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10471725 | HCID 10471725 | 67.1% |
Reaction Steps
2.5 g of 4-diethylaminobenzenesulphonyl chloride are added to a solution comprising 1.17 g of 5-aminovaleric acid and 1.2 g of sodium hydroxide dissolved in 12 cm3 of water, followed by the addition of 12 cm3 of tetrahydrofuran in order to obtain a solution. The mixture is kept stirring for 2 hours at room temperature, 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. 2.2 g of expected product are obtained. M.p. 106°-108° C. After crystallization in an isopropanol/water mixture (1:1), the product, melting point 109°-110° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041436 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-ce59eade854a4733928bad6da208c005 |
| Source note | uspto-grants-1991_08 |