HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 21284374, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 86250420 | HCID 86250420 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 21284374 | HCID 21284374 | — |
Reaction Steps
A mixture of 7.66 g of 1-(1,2,3,6-tetrahydro-1-methyl-4-pyridinyl)ethanone oxime, 6.8 ml of triethylamine, and 3.8 ml of acetyl chloride were stirred at room temperature overnight under a nitrogen atmosphere. Isolation of the product in the conventional manner produced 8.07 g of 1-(1,2,3,6-tetrahydro-4-pyridinyl)ethanone, O-acetyloxime which was converted to the hydrochloride salt, mp 104.5°-105.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04710508 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-56cda14af08443b5a6b8b95e61e41a1e |
| Source note | uspto-grants-1987_12 |