Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410081Generated: November 2, 2026

2-Chloroethanol → HCID 44231692, compound

https://huagongshe.com/reaction/2410081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantPyruvic AcidHCID 1060—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductHCID 44231692HCID 44231692—

Reaction Steps

2-Chloroethyl pyruvate was prepared as follows: pyruvic acid (8.8 g, 100 mmol), 2-chloroethanol (10.45 g, 130 mmol) and p-toluenesulfonic acid monohydrate (1.9 g, 10 mmol) in 40 mL of benzene were heated under reflux with azeotropic dehydration for 5 h. The mixture was cooled to room temperature and diluted with 70 mL of diethyl ether. This organic solution was washed with 100 mL of saturated aqueous NaHCO3 and 100 mL of saturated aqueous NaCl. The organic layer was dried over anhydrous MgSO4, filtered and solvent removed on a rotary evaporator to give 2-chloroethyl pyruvate in quantitative yield, slightly contaminated with benzene and diethyl ether (as determined by 1H NMR). Aliquots used for biological analyses were cleared of diethyl ether and benzene by short path vacuum distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815946B2
Source datasetuspto-grants-2014_08
ORD IDord-33aefec46b94476db85774c3d1968365
Source noteuspto-grants-2014_08