HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 86670539, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86670539 | HCID 86670539 | 44% |
Reaction Steps
To a stirred solution of 1,1-dimethyl-3-butynoic acid (333 mg, 3.0 mmol), azetidine (250 mg, 4.5 mmol) and i-Pr2NEt (1.6 mL, 8.9 mmol) in CH2Cl2 (20 mL) was added solid HATU (1.25 g, 3.3 mmol). The mixture was stirred at rt for 20 h and concentrated to leave a yellow oil. This oil was taken up in EtOAc (100 mL), washed with 5% aq HCl (2×15 mL), satd aq NaHCO3 (15 mL) and brine (15 mL), and dried over Na2SO4. Removal of the solvent left an oil (819 mg) which was purified by chromatography on a 12-g silica cartridge, eluted with a 0-100% EtOAc in hexanes gradient, to afford 1-(azetidin-1-yl)-2,2-dimethylbut-3-yn-1-one (198 mg, 44%) as an oil. 1H NMR (CDCl3) 1.40 (s, 6H), 2.23 (m, 2H), 2.34 (s, 1H), 4.05 (m, 2H), 4.52 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883778B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-5005f355fd2244bbb0528e2facba937d |
| Source note | uspto-grants-2014_11 |