HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373490Generated: October 25, 2026
Pentanal → Cyclopentanone, 2-(1-hydroxypentyl)-
https://huagongshe.com/reaction/1373490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentanal | HCID 8063 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | 2-Pentylidenecyclopentanone | HCID 86000 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cyclopentanone, 2-(1-hydroxypentyl)- | HCID 162060 | 85% |
Reaction Steps
Valeraldehyde having an acid value of 3.4 mg-KOH/g was used as the starting material. 719 g (8.55 mol) cyclopentanone, 325 g water and 2.8 g (0.034 mol) 48% NaOH were introduced into a 2-L four-necked flask, then the mixture was cooled to 15° C. under stirring, and 337 g (3.91 mol) valeraldehyde was added dropwise at the same temperature over 5 hours. Thereafter, the mixture was stirred at the same temperature for 3 hours. After the reaction was finished, the mixture was neutralized and analyzed in the same manner as in Example 1. The result indicated that the reaction mixture contained 562 g (3.30 mol) 2-(1-hydroxy-n-pentyl)cyclopentanone (yield 85.0%) and 9.5 g (0.063 mol) 2-pentylidene cyclopentanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07161041B2 |
|---|
| Source dataset | uspto-grants-2007_01 |
|---|
| ORD ID | ord-89652515fc9d4d4189a64be40abf68a5 |
|---|
| Source note | uspto-grants-2007_01 |
|---|