HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248145Generated: October 27, 2026
1-Bromopropane → 1-[1-(3-Chloro-5-methylphenyl)cyclobutyl]butylamine hydrochloride
https://huagongshe.com/reaction/1248145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-(3-Chloro-5-methylphenyl)-1-cyclobutanecarbonitrile | HCID 21294830 | — |
| Reactant | HCID 178455851 | HCID 178455851 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[1-(3-Chloro-5-methylphenyl)cyclobutyl]butylamine hydrochloride | HCID 13083306 | — |
Reaction Steps
A solution of 1-(3-chloro-5-methylphenyl)-1-cyclobutanecarbonitrile (8.0 g) in ether (40 ml) was added to a solution of propyl magnesium bromide [prepared by the reaction of 1-bromopropane (6.7 g) and magnesium (1.3 g)] in ether (80 ml) and the mixture heated under reflux for two and a half hours. Two thirds of the ether was evaporated off and then, after cooling, a solution of sodium borohydride (3.5 g) in ethanol (150 ml) added. The mixture was maintained at 50° C. for one hour and water (50 ml) and then 5N hydrochloric acid (50 ml) added. The ether layer was separated, dried and evaporated to yield a solid which was recrystallised from propan-2-ol to give 1-[1-(3-chloro-5-methylphenyl)cyclobutyl]butylamine hydrochloride (m.p. 145°-146° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04522828 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-70c06149320242169d141ae7bf792bb2 |
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| Source note | uspto-grants-1985_06 |
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