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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260618Generated: October 30, 2026

Pyridine → HCID 54519927, compound

https://huagongshe.com/reaction/260618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethylene GlycolHCID 8117—
ReactantChloromethyl chloroformateHCID 62754—
SolventDichloromethaneHCID 6344—
ProductHCID 54519927HCID 5451992786.6%

Reaction Steps

Pyridine (0.89 ml, 11.00 mmol) is added dropwise to a solution of chloromethyl chloroformate (1.32 ml, 14.83 mmol) and diethylene glycol (0.47 ml, 5.00 mmol) in dichloromethane (10 ml) at 7° C. with good stirring under a dry N2 atmosphere. After 10 min. at 7° C. and 6 hours at 20° C. the reaction mixture is transferred to a separating funnel with the aid of dichloromethane (10 ml). The reaction mixture is washed with hydrochloric acid (1.00 M, 10 ml), saturated aqueous sodium hydrogen carbonate (10 ml) and water (10 ml). The organic phase is dried (MgSO4) and the solvent evaporated under reduced pressure (10 mm Hg) to give 1.26 g (86%) title product. 1H NMR (300 MHz, CDCl3): δ 3.72 (m, 2×CH2 --O), 4.34 (m, 2×CH2 --O--C=O), 5.71 (s, 2×Cl--CH2 --O). 13C NMR (75 MHz, CDCl3): δ 67.6 (2×CH2 --O), 68.5 (2×CH2 --O--C=O), 72.1 (2×Cl--CH2 --O), 153.2 (2×C=O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05529766
Source datasetuspto-grants-1996_06
ORD IDord-78c5b471e70b4f408299548a43eb7975
Source noteuspto-grants-1996_06