HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29820Generated: October 30, 2026
Diethyl Oxalate → Ethyl 2-(5-acetylamino-2-methylphenyl)-2-oxoacetate
https://huagongshe.com/reaction/29820
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | N-(3-Bromo-4-methylphenyl)acetamide | HCID 11708413 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(5-acetylamino-2-methylphenyl)-2-oxoacetate | HCID 59723642 | 52% |
Reaction Steps
To a solution of N-acetyl-3-bromo-4-methylaniline (1.43 g, 627 mmol) in THF (50 mL) at −78° C. is added 2M BuLi in pentane (7.83 mL, 15.66 mmol) dropwise. After a further 1 h, diethyl oxalate (4.26 mL, 31.3 mmol) is added. After stirring for 4 hours at −78° C., the reaction mixture is quenched with saturated NH4Cl solution. The mixture is partitioned between ethyl acetate and water. The layer is separated and the aqueous layer is extracted with ethyl acetate. The combined organic extracts are washed with brine, dried over Na2SO4, filtered and concentrated. The residue is purified by column chromatography (silica gel, eluting with ethyl acetate; hexanes from 1/1 to 2/1) to afford fee title compound (0.82 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423038B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-c58acdacc1d440f98157c8b743cfb86d |
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| Source note | uspto-grants-2008_09 |
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