HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722682Generated: October 29, 2026
Ammonium Chloride → Diethyl ether 2-propanol
https://huagongshe.com/reaction/722682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | methyl 4-(piperidin-1-ylmethyl)benzoate | HCID 782306 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl ether 2-propanol | HCID 22147583 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07138413B1 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-59844546863a432f9ebdf5181c1fd059 |
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| Source note | uspto-grants-2006_11 |
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