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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386801Generated: October 31, 2026

Diethyl Oxalate → Ethyl 2-pyridineglyoxylate

https://huagongshe.com/reaction/1386801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant2-BromopyridineHCID 7973—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductEthyl 2-pyridineglyoxylateHCID 9989820—

Reaction Steps

A solution of n-butyllithium (100 mL, 1.6 M, 160 mmol) in hexanes was added over 2 min. to a stirred solution of 2-bromopyridine (15.0 mL, 24.9 g, 157 mmol) in 500 mL of ether cooled in a dry ice/i-PrOH bath, causing a temporary rise in temperature to 47° C. After 25 min., the solution was transferred rapidly to a stirred 0° C. solution of diethyl oxalate (75 mL, 81 g, 550 mmol) in 1000 mL of ether. After 2 h at 0° C., the mixture was washed with saturated aq. NaHCO3 (900 ml), water (900 mL), and saturated aq. NaCl (450 mL). The organic layer was dried (MgSO4), filtered, and evaporated. Distillation gave the title compound as 11.68 g of yellow liquid, B.p. 96-108° C. (0.3 mm Hg pressure). For the title compound: 1H NMR (500 MHz, CDCl3) δ 8.78 (d, J=5, 1H), 8.13 (d, J=8, 1H), 7.93 (td, J=8, 2, 1H), 7.56 (ddd, J=8, 5, 1, 11H), 4.51 (q, J=7,22H), 1.44 (t, J=7, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-d5179d9bf4174d9d869d5f827310256b
Source noteuspto-grants-2001_07