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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376172Generated: October 31, 2026

Ammonium Chloride → Diethyl ether 2-propanol

https://huagongshe.com/reaction/1376172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMaleic AcidHCID 444266—
Reactantmethyl 4-(piperidin-1-ylmethyl)benzoateHCID 782306—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl ether 2-propanolHCID 2214758391%

Reaction Steps

4-(Piperidinomethyl)benzoic acid methyl ester (22 mmol) in dry tetrahydrofurane was added dropwise to a suspension of 44 mmol of lithium aluminium hydride in 30 ml of dry tetrahydrofurane at 0° C. After refluxing for 2 hours a saturated solution of ammonium chloride in water was added dropwise. After stirring for 12 hours at ambient temperature the organic layer was isolated and the aqueous layer extracted with methylene chloride. The organic extracts were combined and the solvent was evaporated under reduced pressure. The residue was crystallized with maleic acid from diethyl ether/2-propanol (Yield: 91%). Sodium 4-(piperidinomethyl)benzyl alcoholate (5 mmol) and 6 mmol of 3-phenylpropyl bromide in 10 ml of dry toluene were refluxed for 6 hours. The solvent was evaporated under reduced pressure. The residue was purified by rotatory chromatography on silica gel using methylene chloride/ammonia atmosphere as eluent. The product was crystallized with oxalic acid from diethyl ether/ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169928B2
Source datasetuspto-grants-2007_01
ORD IDord-ff3bfe8c03ff483d9e73b66f2b38bf53
Source noteuspto-grants-2007_01