HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542786Generated: October 31, 2026
Ammonium Chloride → HCID 20207293, compound
https://huagongshe.com/reaction/542786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(3-Bromobenzyl)piperidine | HCID 3847066 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 80236-09-5 | HCID 10630846 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20207293 | HCID 20207293 | — |
Reaction Steps
10.2 g (0.04 mol) of 3-(1-piperidylmethyl)-bromobenzene in 20 ml of tetrahydrofuran are added dropwise to 0.97 g (0.04 mol) of magnesium filings in 5 ml of tetrahydrofuran at a reaction temperature of 60° C. This operation is followed by 30 minutes' stirring at 60° C., and the solution is then cooled to 10° C. 10.2 g (0.04 mol) of 2-benzylaminomethyl-oxirane in 20 ml of tetrahydrofurane are slowly added dropwise and the solution obtained is stirred at room temperature for 2 hours. After the addition of 20 ml of ice water and 4.5 g of ammonium chloride, the aqueous phase is separated and extracted with 25 ml of methylene chloride. The combined organic phases are dehydrated with sodium sulphate and concentrated by evaporation to yield a yellow resin which is chromatographed with methylene chloride/methanol (9:1) against silica gel. After concentration by evaporation, the second fraction yields the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659721 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-749847d6ca77459bb1360b14d8f5eee3 |
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| Source note | uspto-grants-1987_04 |
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