HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388538Generated: October 25, 2026
Ammonium Chloride → alpha-(1-Methyl-4-piperidyl)-2-(2,5-difluorophenylthio)-5-methoxybenzyl alcohol
https://huagongshe.com/reaction/1388538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-chloro-N-methylpiperidine | HCID 79342 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-(2,5-Difluorophenylthio)-5-methoxy-benzaldehyde | HCID 12815952 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | alpha-(1-Methyl-4-piperidyl)-2-(2,5-difluorophenylthio)-5-methoxybenzyl alcohol | HCID 12815955 | 100% |
Reaction Steps
A solution of a Grignard reagent is prepared by a reaction of 6.7 g of 4-chloro-1-methylpiperidine with 1.25 g of magnesium in 40 ml of tetrahydrofuran and is treated while stirring for 10 minutes with a solution of 9.35 g 2-(2,5-difluorophenylthio)-5-methoxy-benzaldehyde in 20 ml of tetrahydrofuran, added dropwise. The mixture is refluxed for 3 hours and, after cooling, it is decomposed with a 20% ammonium chloride solution and extracted with benzene. The extract is washed with water, dried with potassium carbonate and evaporated. There are obtained 12.6 g (100%) of crude oily α-(1-methyl-4-piperidyl)-2-(2,5-difluorophenylthio)-5-methoxybenzyl alcohol which is used in this state for the next reaction. For characterization the crystalline hydrogen oxalate may be prepared by neutralization of a sample with oxalic acid; it is purified by crystallization from acetone and melts at 160°-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04431808 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-b865e5c04b0842d2b4ff341c8bbfda82 |
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| Source note | uspto-grants-1984_02 |
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