HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 86733465, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-{[4-(Bromomethyl)benzoyl]oxy}-N,N,N-trimethylethan-1-aminium bromide | HCID 21535868 | — |
| Reactant | HCID 21535876 | HCID 21535876 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86733465 | HCID 86733465 | — |
Reaction Steps
p-Bromomethyl benzoyl choline bromide (102 mg.) sodium bicarbonate (24.8 mg.) and dimethylsulfoxide (0.3 ml.) are heated in an oil bath at 125° for about 5 minutes until vigorous effervescence ceases. The solution is cooled giving a suspension which upon dilution with 2 ml. of water is dissolved. The addition of 5 ml. of absolute ethanol at room temperature yields a crystalline precipitate which is isolated by centrifugation. The solid is isolated, and dried in vacuo at 75° to yield a crisp glassy solid of hygroscopic character having spectral characteristics indicating the structure of p-formylbenzoyl choline iodide. In accordance with the foregoing procedure but starting with
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959351 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-7c39a15e98dc4b5b93f4170cdccd7be7 |
| Source note | uspto-grants-1976_05 |