HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256191Generated: October 25, 2026
Hydrochloric Acid → Ethyl 4-(4-Methoxybenzyl)acetoacetate
https://huagongshe.com/reaction/256191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Methoxybenzyl bromide | HCID 165021 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Ethyl 4-(4-Methoxybenzyl)acetoacetate | HCID 9992286 | — |
Reaction Steps
Into a 3 l. 3-necked r.b. flask equipped with a mechanical stirrer, thermometer, dropping funnel, and nitrogen gas inlet was placed 24 g. (0.5 mole) of 50% NaH prewashed with hexane, and 1000 ml. of dry tetrahydrofuran. 65 g. (0.5 mole) of ethyl acetoacetate was then added dropwise at -10° to 0° C. using a dry ice-acetone bath. After addition of ethyl acetoacetate was finished, the mixture was gradually warmed up to 10° C. in the course of 15 minutes and then 240 ml. (0.528 mole) of 2.2M n-butyllithium was added dropwise maintaining temperature below -40° to -20° C. After the mixture was stirred at -10° for 15 minutes, 100.5 g. (0.5 mole) of 4-methoxybenzyl bromide was added dropwise over a period of 45 minutes at -10° C. The reaction mixture was gradually warmed up to room temperature and stirred for an additional hour, and then cooled to -20° C. 5N HCl was then carefully added until the solution was slightly acidic.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04701461 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-4961895a58a5443da5f69caf82186bac |
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| Source note | uspto-grants-1987_10 |
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