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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363799Generated: October 29, 2026

Dichloromethane → HCID 178493213, compound

https://huagongshe.com/reaction/2363799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloromethyl-3,4-dimethoxypyridinium chlorideHCID 16216928—
ReactantHCID 178506404HCID 178506404—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
ProductHCID 178493213HCID 17849321383%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

2-Chloromethyl-3,4-dimethoxy pyridine hydrochloride (50 gms), 2-mercapto-5-difluoromethoxy benzimidazole (50 gms) and Tetra butyl ammonium bromide (2 gms) were added under stirring to dichloromethane (300 ml) followed by solution of sodium hydroxide (37.5 gms) in 120 ml water. The contents were then stirred at 25-30° C. for about 12 hours. After reaction completion, the dichloromethane layer was separated, then the aqueous layer was extracted with dichloromethane (60 ml) twice. The organic layers were combined together, water washed and distilled to about 250 ml and cooled to 0° C. 3.5% aqueous sodium hypochlorite solution (464 g) having a sodium hydroxide content of 2.2% was added to the reaction mass, which was maintained at 5-8° C. for about 6 hours. After completion of the reaction; the reaction mass was further cooled to 0 to 5° C. The resulting solid was then filtered and washed with cold acetone (about 100 ml) and dried under vacuum at 35-40° C. to give pantoprazole sodium (75 gms, 83%) of purity greater than 99.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691995B2
Source datasetuspto-grants-2014_04
ORD IDord-7dd17bd702c9451e838584a145265e24
Source noteuspto-grants-2014_04