HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913306Generated: October 30, 2026
Acetic Acid → 8-(3-Ethoxy-4-methyl-benzyl)-1,3,8-triaza-spiro[4.5]decane-2,4-dione
https://huagongshe.com/reaction/913306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3,8-Triazaspiro[4.5]decane-2,4-dione | HCID 120989 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Ethoxy-4-methylbenzaldehyde | HCID 25242058 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-(3-Ethoxy-4-methyl-benzyl)-1,3,8-triaza-spiro[4.5]decane-2,4-dione | HCID 25121956 | 18.1% |
Reaction Steps
To a solution of 1,3,8-triaza-spiro[4.5]decane-2,4-dione (25.4 mg, 0.15 mmol, 1.0 equiv; intermediate A1) in ethanol (1 mL), acetic acid (72.1 mg, 1.2 mmol, 8.0 equiv) and N-ethyl diisopropylamine (77.6 mg, 0.6 mmol, 4.0 equiv) was added 3-ethoxy-4-methyl-benzaldehyde (29.6 mg, 0.18 mmol, 1.2 equiv; intermediate B10, vide infra) and the mixture stirred at 55° C. After 1 h, sodium cyanoborohydride (47.1 mg, 0.75 mmol, 5.0 equiv), dissolved in ethanol (0.5 mL), was added and the mixture stirred at 55° C. over night. Removal of the solvent under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 8.6 mg (17%) of the title compound. MS (ISP): 338.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026365B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-33d0e04fd4f442bf8a2e1974f40931b3 |
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| Source note | uspto-grants-2011_09 |
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