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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373496Generated: October 30, 2026

Phosphoric Acid → Cyclopentanone, 2-(1-hydroxypentyl)-

https://huagongshe.com/reaction/1373496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantPentanalHCID 8063—
ReactantCyclopentanoneHCID 8452—
ReactantSodium HydroxideHCID 14798—
ReactantTrisodium PhosphateHCID 24243—
Catalyst2-PentylidenecyclopentanoneHCID 86000—
ProductCyclopentanone, 2-(1-hydroxypentyl)-HCID 16206084.5%

Reaction Conditions

Temperature15 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07161041B2
Source datasetuspto-grants-2007_01
ORD IDord-c3f49d2bbeeb4729bbe7286ec7b79832
Source noteuspto-grants-2007_01