HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443329Generated: October 29, 2026
Benzaldehyde → 2-(2-Hydroxy-2-phenylethyl)-3,5,6-trimethylpyrazine
https://huagongshe.com/reaction/443329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetramethylpyrazine | HCID 14296 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Hydroxy-2-phenylethyl)-3,5,6-trimethylpyrazine | HCID 585936 | — |
Reaction Steps
A solution of phenyllithium in benzene-ether (90 milliliters, 0.095 mole) was diluted with 100 milliliters anhydrous ether and cooled to 0° C. A solution of 13.6 grams tetramethylpyrazine (0.1 mole) in 50 milliliters ether was added slowly to the phenyllithium solution. The reaction mixture was stirred at room temperature for 2 hours and heated under reflux for 1 hour. The mixture was allowed to cool to room temperature and a solution of 10 grams of freshly distilled benzaldehyde (0.1 mole) in 50 milliliters of ether was added dropwise. The mixture was stirred at room temperature for an additional 1.5 hours and cooled to 0° C. Water was added, and the organic phase was separated and washed three times with water. The recovered water extracts were washed with methylene chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259969 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-3997c429ec9e458fb0ee6a743cbde9bc |
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| Source note | uspto-grants-1981_04 |
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