HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248568Generated: November 1, 2026
5-Aminovaleric acid → HCID 10427381, compound
https://huagongshe.com/reaction/2248568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminovaleric acid | HCID 138 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10377881 | HCID 10377881 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10427381 | HCID 10427381 | 56.9% |
Reaction Steps
7.8 g of 4-piperidinylbenzenesulphonyl chloride are added to a solution comprising 3.51 g of 5-aminovaleric acid and 3.6 g of sodium hydroxide dissolved in 35 cm3 of water, followed by the addition of 35 cm3 of tetrahydrofuran in order to obtain a solution. The temperature rises to 35° C. The mixture is kept stirring for 4 hours at room temperature, the tetrahydrofuran is evaporated off, the reaction medium is acidified using acetic acid, diluted with 100 cm3 of water and extracted with chloroform, the organic phase is dried and the solvents are removed under reduced pressure. 5.8 g of expected product are obtained. M.p. 115°-120° C. After crystallization in an isopropanol/water mixture (1:1), the product, melting point 120°-122° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05041436 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-ddc3de11d0744bf185201636b616ea14 |
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| Source note | uspto-grants-1991_08 |
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