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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 1-Azaspiro(4.5)-decane-2,8-dione | HCID 11412594 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,4-Dioxa-9-azadispiro[4.2.4.2]tetradecan-10-one | HCID 11183437 | 95.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416141B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-0284f867e9874b56890f4ad0522708da |
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| Source note | uspto-grants-2016_08 |
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