Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410480Generated: October 31, 2026

Ethyl Acetate → Ethyl [5-oxooctahydropentalen-2-yl]acetate

https://huagongshe.com/reaction/410480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactantethyl[5,5-dimethylhexahydro-1'H-spiro[1,3-dioxane-2,2'-pentalen]-5'-yl]acetateHCID 86731803—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductEthyl [5-oxooctahydropentalen-2-yl]acetateHCID 6724963413.4%

Reaction Steps

A solution of the product of Step 3 (400 mg, 1.350 mmol) in acetone (8.0 mL) and water (8.00 mL) was stirred at room temperature 16 hrs with p-toluenesulfonic acid monohydrate (257 mg, 1.35 mmol). The volatiles were removed under reduced pressure and the residue was partitioned between EtOAc and brine. The separated organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. Flash chromatography (10 to 60% EtOAc in hexanes) afforded ethyl[5-oxooctahydropentalen-2-yl]acetate (38 mg, 0.181 mmol, 13.4% yield) as a colorless oil. 1H NMR (500 MHz, CDCl3) δ 4.14-4.09 (m, 2H), 2.73-2.71 (m, 2H), 2.53-2.47 (m, 2H), 2.37-2.32 (m, 3H), 2.29-2.25 (m, 2H), 2.08-2.02 (m, 2H), 1.27-1.24 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-3136d2edc89f480baeee320f3ad7b431
Source noteuspto-grants-2014_06