HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516871Generated: October 30, 2026
Acetone → Benzyl 2-(4-oxocyclohexyl)acetate
https://huagongshe.com/reaction/516871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Benzyloxycarbonylmethylcyclohexanone ethylene acetal | HCID 59009026 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 2-(4-oxocyclohexyl)acetate | HCID 58069819 | 86% |
Reaction Steps
p-Toluene sulfonic acidmonohydrate (207 mg, 1.21 mmol) was added to a mixture composed of benzyl 2-(1,4-dioxaspiro[4,5]decan-8-yl)acetate (7.0 g, 24.11 mmol), acetone (220 ml), and water (10 ml) at room temperature, and the mixture was stirred at 55° C. for 15 hr. The mixture was cooled with ice and was adjusted to pH 5 by the addition of solid sodium bicarbonate. The mixture was concentrated under reduced pressure, and the residue was chromatographed on silica gel column (hexane:ethyl acetate=85:15) to give the title compound as a colorless solid (5.1 g, yield 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09115079B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-ab00941a8c2d4cb3b0906026b9e29da9 |
|---|
| Source note | uspto-grants-2015_08 |
|---|