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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619735Generated: November 1, 2026

Ammonium Chloride → HCID 59830372, compound

https://huagongshe.com/reaction/1619735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59830372HCID 59830372—

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium tert-butylate (2.1 g, 18.8 mmol, dissolved in 20 ml abs. THF) was added within 30 min to a suspension of methyltriphenylphosphonium bromide (7.5 g, 21 mmol) in dry THF (20 ml) under argon at 0° C. The reaction mixture was stirred for 30 min at 0° C. before 1-benzyl-3-methylpiperidin-4-one (3.05 g, 15 mmol, dissolved in abs. THF (20 ml)) was added dropwise within 30 min at 0° C. The reaction mixture was stirred for 30 min at 0° C. and brought to RT within 1 h and stirred for a further 15 h. For working up, the mixture was added to sat. NH4Cl solution (50 ml) and then extracted with EtOAc (3×20 ml). The desired product S was converted into the corresponding hydrochloride by extraction with 2 N HCl solution (20 ml). The organic phase was washed with water (3×20 ml) and the combined aqueous phases were basified with K2CO3. The product S was obtained in the form of a layer of oil and was separated off by reextraction with EtOAc (3×20 ml). After drying of the combined organic phases over Na2SO4 and removal of the solvent, the desired product S was present in a sufficiently pure form (2.50 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772307B2
Source datasetuspto-grants-2014_07
ORD IDord-7a041af5cb4c41a68da7395de3ea7af2
Source noteuspto-grants-2014_07