HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322930Generated: October 27, 2026
Hydrochloric Acid → Ethyl 4-benzyloxyphenyl-2,4-dioxobutanoate
https://huagongshe.com/reaction/322930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 1-[4-(Benzyloxy)phenyl]ethan-1-one | HCID 245226 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-benzyloxyphenyl-2,4-dioxobutanoate | HCID 86756594 | 97.1% |
Reaction Steps
Diethyl oxalate (17.7 g) is added in one portion to a stirred suspension of potassium ethoxide (10.2 g) in anhydrous ether (1000 mL). The stirred mixture is cooled to 0° C., treated with 4-benzyloxyacetophenone (25 g) portionwise, and stirring continued for 3 hours. After standing at room temperature for 18 hours the reaction mixture is poured onto 1 N hydrochloric acid (500 mL) and the organic phase separated. The organic phase is washed with water, dried over magnesium sulphate and evaporated to give ethyl 4-benzyloxypheyl-2,4-dioxobutanoate (35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211234B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-ac3842eed7fe49118cd750bc229b0c1c |
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| Source note | uspto-grants-2001_04 |
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