HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732567Generated: October 26, 2026
Hydrochloric Acid → Methyl 1-(2-chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride
https://huagongshe.com/reaction/1732567
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chlorobenzyl chloride | HCID 11906 | — |
| Reactant | Norarecoline Hydrochloride | HCID 201540 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 1-(2-chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride | HCID 12769333 | 98.1% |
Reaction Steps
Triethylamine (2.2 g.) and 2-chlorobenzyl chloride (1.63 g.) were added to a solution of methyl 1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride (1.63 g.) in methanol (10 ml.). The solution obtained was kept for 24 hours at 20°-25° C. and then evaporated. Water (20 ml.) and 10% w/v sodium carbonate solution were then added to the residue to give a mixture of pH 10. This mixture was extracted with ether (2×20 ml.). The combined extracts were washed with water, dried (MgSO4) and evaporated. The residual oil was dissolved in acetone to give a solution which was treated with a slight excess of ethereal hydrogen chloride. The solid which precipitated was collected by filtration and washed with acetone to give methyl 1-(2-chlorobenzyl)-1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride (1.5 g.) m.p. 171°-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04238488 |
|---|
| Source dataset | uspto-grants-1980_12 |
|---|
| ORD ID | ord-ef6a323c0a934e0eb80c165241e4f9cc |
|---|
| Source note | uspto-grants-1980_12 |
|---|