HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13154060, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13154059 | HCID 13154059 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13154060 | HCID 13154060 | — |
Reaction Steps
20.4 g (0.2 mol) of acetic anhydride are added dropwise to a solution of 19.5 g (0.1 mol) of 4-methoxy-5-n-butyl-2-picoline-N-oxide in 100 ml of toluene over the course of 15 minutes, whilst stirring. Thereafter the mixture is heated for 8 hours under reflux. After evaporation to dryness in vacuo, the mixture is rendered alkaline with 2 N aqueous sodium carbonate solution and is extracted with ether. The ether phases are combined, dried with sodium sulphate, filtered and evaporated. Distillation of the residue in a bulb tube in a high vacuum at 120° yields 2-acetoxymethyl-4-methoxy-5-n-butyl-pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998955 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-e874a6d5719e4183a7c44ac338061d01 |
| Source note | uspto-grants-1976_12 |