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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214643Generated: October 30, 2026

Dimethyl oxalate → HCID 69655528, compound

https://huagongshe.com/reaction/2214643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl oxalateHCID 11120—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 21947396HCID 21947396—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69655528HCID 6965552853%

Reaction Conditions

Temperature0 °C

Reaction Steps

N,N-Bis-(4-fluoro-benzyl)-acetamide (15.0 grams, 54.5 mmol) and dimethyloxalate (9.6 grams, 81.3 mmol) were dissolved in 54 mL of THF. After cooling to 0° C. 108 mL of 1N LiHMDS (THF) was added dropwise. The reaction mixture was stirred 1 hr then quenched with 1N HCl. The resulting mixture was extracted with CH2Cl2, dried over Na2SO4, filtered and the solvent removed under vacuum. The product was purified by flash column chromatography (SiO2, 80:20 hexanes/EtOAc) to yield 10 grams (53% yield) of 3-[bis-(4-fluoro-benzyl)-carbamoyl]-2-hydroxy-acrylic acid methyl ester as a solid. Mp=118–120° C. Anal. calcd for C19H17F2NO4: C, 63.15; H, 4.74; N, 3.87. found: C, 62.97; H, 4.72; N, 3.81. 1H NMR (500 MHz, CDCl3) δ: 3.87 (s, 3), 4.46 (s, 2), 4.58 (s, 2), 6.32 (s, 1), 7.00–7.26 (overlapping m, 8). 13C NMR (125 MHz, CDCl3) δ: 47.34, 49.35, 53.03, 93.34, 115.66, 115.83, 116.00, 116.18, 128.45, 128.52, 130.03, 130.10, 131.09, 131.93, 131.95, 160.29, 161.44, 161.51, 163.10, 163.41, 163.47, 171.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109186B2
Source datasetuspto-grants-2006_09
ORD IDord-35d684e30ce548869cdcb96c9bef2c9e
Source noteuspto-grants-2006_09