HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373496Generated: October 30, 2026
Phosphoric Acid → Cyclopentanone, 2-(1-hydroxypentyl)-
https://huagongshe.com/reaction/1373496
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Pentanal | HCID 8063 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trisodium Phosphate | HCID 24243 | — |
| Catalyst | 2-Pentylidenecyclopentanone | HCID 86000 | — |
| Product | Cyclopentanone, 2-(1-hydroxypentyl)- | HCID 162060 | 84.5% |
Reaction Steps
The aqueous layer and the distilled fraction of (b) were introduced into a 500-mL four-necked flask and then 48.2 g cyclopentanone (1.34 mol including a re-used cyclopentanone) and 1.96 g (0.0236 mol) 48% NaOH, including NaOH for converting phosphoric acid contained in the aqueous layer to trisodium phosphate were added thereto. The mixture was cooled to 15° C. under stirring, and 50.0 g (0.58 mol) valeraldehyde was added dropwise at the same temperature over 5 hours. Thereafter, the mixture was stirred at the same temperature for 2 hours. After the reaction was finished, the mixture was neutralized with 1.89 g (0.0203 mol) 105% condensed phosphoric acid and separated into two phases at 40° C. The pH of the aqueous layer was 5.5. The resulting organic layer was 170.7 g, and the aqueous layer was 4.72 g. The organic layer was analyzed in the same manner as in Example 1. The result indicated that the reaction mixture contained 82.4 g (0.484 mol) 2-(1-hydroxy-n-pentyl)cyclopentanone (yield 83.5%) and 2.25 g (0.015 mol) 2-pentylidene cyclopentanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07161041B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-c3f49d2bbeeb4729bbe7286ec7b79832 |
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| Source note | uspto-grants-2007_01 |
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