HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloromethyl acetate → 1-(Acetyloxymethyl)-3-(dimethylcarbamoyloxy)pyridinium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloromethyl acetate | HCID 69366 | — |
| Reactant | Norpyridostigmine | HCID 98821 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(Acetyloxymethyl)-3-(dimethylcarbamoyloxy)pyridinium chloride | HCID 13881950 | 93.3% |
Reaction Steps
3-Dimethylcarbamoyloxypyridine (1.66 g) and chloromethyl acetate (2.18 g) were stirred at 90° C. for 1 hr. The hot reaction mixture was poured into 100 ml of anhydrous diethylether with vigorous stirring. The supernatant was removed by decantation followed by addition of 500 ml of diethylether. Again, the supernatant was removed by decantation. These procedures were repeated three times. The solvent was removed under reduced pressure to give 2.56 g of 1-(acetyloxymethyl)-3-(dimethylcarbamoyloxy)pyridinium chloride as oil. The structure was determined by N.M.R.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04661502 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-7ef6bae101fb49ba8a089e1413a13140 |
| Source note | uspto-grants-1987_04 |