HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078258Generated: November 1, 2026
(Z)-Benzaldehyde oxime → HCID 67099912, compound
https://huagongshe.com/reaction/2078258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Z)-Benzaldehyde oxime | HCID 12143 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 67099495 | HCID 67099495 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67099912 | HCID 67099912 | — |
Reaction Steps
A solution of benzaldehyde oxime (0.16 g, 1.3 mmol) in DMF (3 mL) was added dropwise to a stirred suspension of 60% NaH (0.033 mL, 1.3 mmol) in dry 1,4-dioxane (5 mL) under a nitrogen atmosphere at room temperature. After 30 minutes, a solution of ethyl 3-(5-chloro-2-(2-cyano-1-ethoxy-1-oxopropan-2-yl)phenyl)propiolate (0.445 g, 1.3 mmol) in DMF (3 mL) was added dropwise. The reaction was monitored by LC-MS and, when complete, the solvent was removed. The residual brown oil was dissolved in DCM (50 mL), water (30 mL), and AcOH (2 mL). The layers were separated, and the aqueous layer was extracted with DCM (3×30 mL). The combined organic layers were dried with MgSO4 and concentrated in vacuo. The crude residue was purified using silica flash chromatography with a gradient of 10-50% EtOAc/hexanes. MS m/e=306 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928139B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-85d763f57a574b52b79dd82ed074e76f |
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| Source note | uspto-grants-2011_04 |
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