HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857731Generated: October 26, 2026
Sulfuric Acid → ethyl 2-(3-chlorophenyl)-2-oxoacetate
https://huagongshe.com/reaction/857731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 178478127 | HCID 178478127 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | ethyl 2-(3-chlorophenyl)-2-oxoacetate | HCID 2758814 | 101.2% |
Reaction Steps
Diethyl oxalate (4.4 g, 30.2 mmol) was dissolved in dry ethyl ether (30 mL) and freshly distilled THF (30 mL) and cooled to −78° C. with stirring, under a nitrogen atmosphere. Then added 3-chlorophenylmagnesium bromide (0.5 M in THF, 72.5 mL, 36.2 mmol) dropwise, via an addition funnel, while keeping the temperature between −75 to −78° C. The addition took approximately 90 minutes. After 3 hours, the reaction was quenched by the dropwise addition of 2N sulfuric acid (50 mL, 91 mmol) at −78° C. and upon completion of the addition, the mixture was allowed to return to room temperature. The mixture was extracted with ethyl ether (3×) and the combined ether extracts were washed with brine (2×), dried over magnesium sulfate, filtered, evaporated in vacuo and vacuum-dried to yield ethyl-(3-chlorophenyl)(oxo)acetate (6.5 g, HPLC RT=3.46 min, Method A; LCMS m/z=213).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07144899B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-aaf32d1302a34c4a84f09df8c0a7c47f |
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| Source note | uspto-grants-2006_12 |
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