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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388241Generated: November 2, 2026

Diethyl Oxalate → HCID 67529552, compound

https://huagongshe.com/reaction/2388241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant1-Cyclohexylpropan-1-oneHCID 70748—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventDiethyl EtherHCID 3283—
ProductHCID 67529552HCID 6752955262.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

LHMDS solution (39.3 mL, 39.3 mmol, 1M in hexanes) was added to 200 mL of diethyl ether and the mixture was cooled to −78° C. Cyclohexyl ethyl ketone (5.0 g, 35.7 mmol) dissolved in 50 mL of ether was added dropwise, and the resulting mixture was stirred at −78° C. for 1 h. Diethyl oxalate (5.6 mL, 41.1 mmol) was then added dropwise, and the cooling bath was removed and the mixture was allowed to come to room temperature. After the mixture was stirred for 16 h, 1M hydrochloric acid (200 mL) was added and the organic layer was separated. The aqueous layer was extracted with CH2Cl2 (3×100 mL) and the combined organic layers were dried over MgSO4 and concentrated. The crude oil was purified by chromatography (0-20% EtOAc/hexanes) to give 5.36 g of the title compound. MS: (−) m/z 239.33 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269008B2
Source datasetuspto-grants-2012_09
ORD IDord-d782036cd55c402580ddebea6f1d6879
Source noteuspto-grants-2012_09