HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26175Generated: October 30, 2026
Hydrochloric Acid → gamma-(4-Benzyl-4-hydroxypiperidino)-2-chlorobutyrophenone hydrochloride
https://huagongshe.com/reaction/26175
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | gamma-(4-Benzyl-4-hydroxypiperidino)-2-aminobutyrophenone | HCID 21324676 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | gamma-(4-Benzyl-4-hydroxypiperidino)-2-chlorobutyrophenone hydrochloride | HCID 86736453 | — |
Reaction Steps
To a cooled solution of 3.6 g of γ-(4-benzyl-4-hydroxypiperidino)-2-aminobutyrophenone in 35 ml of 2N hydrochloric acid was added dropwise a solution of 0.74 g of sodium nitrite in 5 ml of water with stirring below 0° C. The resulting diazonium salt solution was added all at once to a cold suspension of 1.5 g of cuprous chloride in 5 ml of concentrated hydrochloric acid with vigorous stirring. The mixture was stirred for 30 minutes under cooling with ice, and stirring was continued for 2 hours at room temperature and then for 1 hour at 55°-60° C. After cooling, the reaction mixture was made alkaline, and extracted with chloroform. The extract was washed with water, dried and concentrated to a residue. The residue was treated with methanolic hydrogen chloride and recrystallization of the resulting solid matter from isopropanol gave γ-(4-benzyl-4-hydroxypiperidino)-2-chlorobutyrophenone hydrochloride.8c
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04148796 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-72b3ad87da5a47c7958a2a715a962bb0 |
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| Source note | uspto-grants-1979_04 |
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