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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982001Generated: October 29, 2026

Toluene → HCID 53690215, compound

https://huagongshe.com/reaction/982001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantChloromethyl ethyl etherHCID 18523—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22158922HCID 22158922—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53690215HCID 5369021572.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

10.65 g of a 80% suspension of sodium hydride in liquid paraffin are suspended in 300 ml of anhydrous tetrahydrofuran. A solution of 120 g of 3-methyl 5-(2-bromoethyl) (±)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-pyridine-3,5-dicarboxylate and 28.4 g of chloromethyl ethyl ether in 300 ml of anhydrous tetrahydrofuran is slowly added dropwise in the course of 4 h at -5° to -7° C., while stirring. After the mixture has been stirred for a further hour at 0° C., 600 ml of toluene and 210 ml of water are added in succession. The phases are separated, and the organic phase is washed with water, dried overnight and evaporated in vacuo. The residue is dissolved in 390 ml of warm ethanol and the stirred solution is then cooled. The product crystallises out during this procedure. It is cooled to 0° C., filtered off under suction, washed with ice-cold ethanol and dried. 98.5 g of the title compound of m.p. 72.5°-74° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994461
Source datasetuspto-grants-1991_02
ORD IDord-5b0fe68cef354ac0b1f567bc5a1c4be7
Source noteuspto-grants-1991_02