HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851140Generated: October 31, 2026
Ammonium Hydroxide → 3-[1-(2-Phenylethyl)-1,2,5,6-tetrahydropyridin-3-yl]phenol
https://huagongshe.com/reaction/851140
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 5-(3-Methoxyphenyl)-1-(2-phenylethyl)-1,2,3,6-tetrahydropyridine | HCID 13234203 | — |
| Reactant | Pyridinium hydrochloride | HCID 21584435 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[1-(2-Phenylethyl)-1,2,5,6-tetrahydropyridin-3-yl]phenol | HCID 13234204 | 85.8% |
Reaction Steps
A mixture of 6 g of the product of Step A and 12 g of pyridinium hydrochloride was heated at 200° C. with stirring for 21/2 hours and the mixture was cooled and diluted with water. Ammonium hydroxide was added to the mixture which was then extracted with methylene chloride. The organic phase was washed with water, dried and evaporated to dryness. The residue was chromatographed over silica gel and was eluted with an 8-2 chloroform-acetone mixture to obtain 4.9 g of 3-(1-phenethyl-1,2,5,6-tetrahydropyridin-3-yl)-phenol melting at 155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382942 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-7b58f8ff1c0e41b0a9593bb9cc60ef3f |
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| Source note | uspto-grants-1983_05 |
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