HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178443160, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20516628 | HCID 20516628 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178443160 | HCID 178443160 | — |
Reaction Steps
To a solution of 14.6 g of o-tetradecyloxyphenacylbromide in 75 ml of acetonitrile was added a solution of 2.8 g of tetrazole and 4.0 g of triethylamine in 75 ml of acetonitrile. The reaction mixture was stirred at reflux temperature for 2 hours then evaporated to dryness. The residue was dissolved in chloroform and the organic layer washed with water, dried over magnesiumsulfate, filtered and evaporated to give the crude compound. Recrystallisation from petrol (b.p. 60°-80° C.) gave the acetophenone derivative as a fine white powder. Yield: 12.7 g; m.p. 67° to 69° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226934 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-1c134ee3be2a42ecaedc855b2a855812 |
| Source note | uspto-grants-1980_10 |