HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzaldehyde → 2-(2-Hydroxy-2-p-methylphenylethyl)-3,5,6-trimethylpyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Tetramethylpyrazine | HCID 14296 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Hydroxy-2-p-methylphenylethyl)-3,5,6-trimethylpyrazine | HCID 585937 | 42% |
Reaction Steps
To a solution of phenyllithium in 150 milliliters 7:3 benzene-ether (0.1 mole) at 0° C. was slowly added a solution of 13.6 grams of tetramethylpyrazine (0.1 mole). The mixture was stirred at room temperature for 2 hours and heated under reflux for 1.5 hours. The mixture was cooled to 0° C., and a solution of 12.0 grams of p-tolualdehyde (0.1 mole) in 50 milliliters of ether was added dropwise. The reaction mixture was stirred at room temperature for 1 hour and then treated in the manner of Example I. The crude product was crystallized from ether to yield 10.7 grams of product (42%) as fine white needles, m.p. 99°-101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259969 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-320ce71e049946c08c23a48154977ae4 |
| Source note | uspto-grants-1981_04 |