HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846784Generated: October 30, 2026
Potassium Iodide → HCID 19883499, compound
https://huagongshe.com/reaction/846784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(3-Chloropropoxy)-4-fluorobenzene | HCID 74391 | — |
| Reactant | HCID 19883537 | HCID 19883537 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19883499 | HCID 19883499 | 75% |
Reaction Steps
A mixture of 7.5 parts of 1-(3-chloropropoxy)-4-fluorobenzene, 10.5 parts of N,N-diethyl-2-[(4,4-dimethoxy-3-piperidinyl)oxy]ethanamine, 7 parts of N,N-diethylethanamine, 1 part of potassium iodide and 90 parts of N,N-dimethylformamide was stirred for 17 hours at 60° C. The reaction mixture was poured onto water and the product was extracted with trichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) saturated with ammonia, as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the hydrochloride salt in acetonitrile and 2-propanol. The whole was evaporated and the residue was taken up in acetonitrile. The solution was evaporated, yielding 14 parts (75%) of N,N-diethyl-2-[[1-[3-(4-fluorophenoxy)propyl]-4,4-dimethoxy-3-piperidinyl]oxy]ethanamine as a residue (intermediate 115).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137896 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-fca75b8e08794b8a8631a14c967b2ddd |
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| Source note | uspto-grants-1992_08 |
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