HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309180Generated: October 26, 2026
Triethylamine → N-(phenoxycarbonylamino)-1,2,3,6-tetrahydropyridine
https://huagongshe.com/reaction/2309180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 1,2,3,6-Tetrahydropyridin-1-amine hydrochloride | HCID 19376047 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(phenoxycarbonylamino)-1,2,3,6-tetrahydropyridine | HCID 20152376 | 92.1% |
Reaction Steps
To a solution of N-amino-1,2,3,6-tetrahydropyridine hydrochloride (1.346 g) and triethylamine (2.024 g) in methylene chloride (60 ml) was added a solution of phenyl chloroformate (1.566 g) in methylene chloride (40 ml) and the mixture was stirred for 4 hours at 5° C. Evaporation of the solvent gave a residue, which was extracted with ethyl acetate (150 ml). The extract was washed with water and dried over magnesium sulfate. The solvent was evaporated in vacuo to give N-(phenoxycarbonylamino)-1,2,3,6-tetrahydropyridine (2.01 g), which was recrystallized from diisopropyl ether to give the desired compound (0.732 g) as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04694004 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-5a5455e251314c13b390d0213407f274 |
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| Source note | uspto-grants-1987_09 |
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