HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759356Generated: October 31, 2026
5-Aminovaleric acid → HCID 20531976, compound
https://huagongshe.com/reaction/1759356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminovaleric acid | HCID 138 | — |
| Reactant | Stearyl Alcohol | HCID 8221 | — |
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20531976 | HCID 20531976 | 90% |
Reaction Steps
A mixture of 5.05 gm (43.1 mmole) of 5-aminopentanoic acid, 23.3 gm (86.1 mmole) of stearyl alcohol, and 12.0 gm (63.1 mmole) of p-toluenesulfonic acid monohydrate in 200 ml of toluene was heated at reflux, using a Dean-Stark trap to remove water. After 90 minutes, the solution was allowed to cool to 0° C., giving a heavy gelatinous precipitate. The crude ester was collected, washed thoroughly with toluene, triturated with diethyl ether, and dried in vacuo to give 21.1 gm (38.8 mmole) of fluffy white octadecyl 5-aminopentanoate as the tosylate salt. The ester was sufficiently pure according to nmr spectroscopy (in (CD3)2SO) for subsequent use without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04340730 |
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| Source dataset | uspto-grants-1982_07 |
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| ORD ID | ord-6df66363fc4e42b4b86d5c70159947cb |
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| Source note | uspto-grants-1982_07 |
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