HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920584Generated: October 26, 2026
Sodium Iodide → 3-[2-(4-Octyloxy-phenyl)-morpholin-4-yl]-butyric acid tert-butyl ester
https://huagongshe.com/reaction/920584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Tert-butyl 3-bromobutanoate | HCID 57092335 | — |
| Reactant | 2-(4-Octyloxy-phenyl)-morpholine | HCID 67032351 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-[2-(4-Octyloxy-phenyl)-morpholin-4-yl]-butyric acid tert-butyl ester | HCID 67032485 | 31.4% |
Reaction Steps
A mixture of 2-(4-octyloxy-phenyl)-morpholine (0.24 gram, 1.1 mmol), 3-bromobutyric acid tert-butyl ester (0.24 g; 1.1 mmol), sodium iodide (27.4 mg; 0.2 mmol), and DBU (0.4 mL; 2.7 mmol) in CH3CN (10 mL) was heated in a closed vessel at 120° C. After cooling to RT the reaction mixture was partitioned between 5% aqueous NaHCO3 solution and EtOAc. The layers were separated and the organic layer was dried (Na2SO4), filtered, and concentrated. The residue was purified by column chromatography (SiO2, Et2O) to afford 3-[2-(4-octyloxy-phenyl)-morpholin-4-yl]-butyric acid tert-butyl ester (0.15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273017B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-90581374fad244ec972668292d2ee387 |
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| Source note | uspto-grants-2016_03 |
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