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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280862Generated: October 30, 2026

Diethyl Oxalate → HCID 89370582, compound

https://huagongshe.com/reaction/2280862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
ReactantEthanone, 1-(3-methylenecyclobutyl)- (9CI)HCID 45084997—
SolventEthanolHCID 702—
ProductHCID 89370582HCID 89370582—

Reaction Steps

Sodium (1.15 g, 49.9 mmol) was dissolved in dry EtOH (30 mL, denaturated with 5% diethylether). Compound 8a (5.5 g, 49.9 mmol, crude) was dissolved in dry EtOH (45 mL) and the above prepared sodium ethoxide solution was added. This mixture was stirred at rt for 15 min and then diethyl oxalate (6.8 mL, 49.9 mmol) was added dropwise. The reaction mixture was placed in a pre-heated (to 67° C.) oil bath and stirred at this temperature for 4.5 h. The mixture was left at rt overnight. The solvent was removed, EA (100 mL) and 1 M HCl (70 mL) were added and organic phase was separated. The aq. phase was re-extracted with EA (50 mL). The combined organic phases were washed with water, brine and dried over anh. Na2SO4. The solvent was removed under reduced pressure and the residue was purified on silica using hexanes/MTBE 9:1 as eluent giving pure product 8b. Yield: 6.29 g, 56% over two steps. 1H-NMR (CDCl3), δ (ppm): 6.36 (s, 1H), 4.85-4.80 (m, 2H), 4.34 (q, J=8.0 Hz, 2H), 3.35-3.25 (m, 1H), 3.05-2.85 (m, 4H), 1.36 (t, J=8.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139539B2
Source datasetuspto-grants-2015_09
ORD IDord-79ba2ce61ecd40538ddd16aa0df027ac
Source noteuspto-grants-2015_09