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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483218Generated: October 31, 2026

Ethylene Glycol → 1,4-Dioxa-9-azadispiro[4.2.4.2]tetradecan-10-one

https://huagongshe.com/reaction/1483218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant1-Azaspiro(4.5)-decane-2,8-dioneHCID 11412594—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product1,4-Dioxa-9-azadispiro[4.2.4.2]tetradecan-10-oneHCID 1118343795.1%

Reaction Steps

A stirred mixture of 1-azaspiro[4.5]decane-2,8-dione (P1, 2.00 g, 12.0 mmol), ethylene glycol (2.96 g, 47.7 mmol), and 4-methylbenzenesulfonic acid (100 mg, 0.735 mmol) in toluene (100 mL) was refluxed for 20 h with Dean-Stark apparatus to remove water. After this time, the reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was mixed with saturated aqueous sodium bicarbonate (100 mL) and the resulting aqueous mixture was extracted with 5% methanol/ethyl acetate (4×150 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford compound P2 as an off-white solid (2.41 g, 95%): 1H NMR (300 MHz, DMSO-d6) δ 5.82 (bs, 1H), 3.95 (s, 4H), 2.41 (t, J=8.0 Hz, 2H), 1.99 (t, J=8.0 Hz, 2H), 1.80-1.65 (m, 8H). MS (M+H) 212.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416141B2
Source datasetuspto-grants-2016_08
ORD IDord-0284f867e9874b56890f4ad0522708da
Source noteuspto-grants-2016_08