HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170731Generated: October 31, 2026
Ethyl Acetoacetate → HCID 70976343, compound
https://huagongshe.com/reaction/2170731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70976343 | HCID 70976343 | 90% |
Reaction Steps
Ethyl acetoacetate (0.632 mL, 5 mmol) was added to a solution containing NaH (0.493 g, 11.25 mmol) in DMF (5 mL), and the resulting mixture was stirred at 0° C. for 30 minutes. 1-bromo-4-(bromomethyl)benzene (2.788 g, 11.15 mmol) was added to the mixed liquid, and the resulting mixture was stirred at room temperature for 12 hours. The mixed liquid was then poured into a saturated aqueous solution of NaHCO3, and extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, dried using MgSO4, and then concentrated under reduced pressure, yielding the title compound (4k) in a yield of 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051246B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-a7d09c4e373e4a318d3ed43f0b8dc2ce |
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| Source note | uspto-grants-2015_06 |
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