HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466973Generated: October 31, 2026
Ethyl Acetoacetate → HCID 66746746, compound
https://huagongshe.com/reaction/1466973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 3-(3-Amino-2-cyanophenoxy)-2,2-dimethyl-N-propylpropanamide | HCID 46833662 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66746746 | HCID 66746746 | 84.1% |
Reaction Steps
To a solution of 3-(3-amino-2-cyanophenoxy)-2,2-dimethyl-N-propylpropan-amide (Tachdjian, C. et al. PCT Int. Appl. 2008, WO 2008154221, 1.38 g, 5.0 mmol) and ethyl acetoacetate (0.66 g, 5.0 mmol) in dry toluene (150 mL) was added SnCl4 (2.61 g, 10.0 mmol) dropwise via syringe at room temperature under nitrogen. After 1 hr at room temperature, the reaction mixture was refluxed for an additional 5 hrs. The solution was cooled to room temperature and the solvent removed under reduced pressure. The residue was diluted with EtOAc, and aqueous NaOH (2N) was added at room temperature to pH>8. The solution was filtered and the organic layer separated. The aqueous layer was extracted with EtOAc (5×). The combined organic layers was washed with brine, and dried over Na2SO4. After evaporation of the solvent, the residue was purified by chromatography on silica gel (0.5% MeOH in EtOAc) to give the title compound as an off-white solid (1.63 g, 84%). 1H NMR (400 MHz, DMSO-d6) δ 0.73 (t, J=7.6 Hz, 3H), 1.25 (s, 6H), 1.32 (t, J=7.4 Hz, 3H), 1.35-1.42 (m, 2H), 2.54 (s, 3H), 3.00-3.05 (m, 2H), 4.12 (s, 2H), 4.31 (q, J=7.4 Hz, 2H), 6.87 (d, J=8.0 Hz, 1H), 7.23 (d, J=8.0 Hz, 1H), 7.50 (t, J=8.0 Hz, 1H), 7.80 (t, J=5.6 Hz, 1H), 8.08 (s, 2H). MS 388 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000054B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-9c08ba8c7ec64f6f86fdac129c47586b |
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| Source note | uspto-grants-2015_04 |
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