HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 18960342, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 18960337 | HCID 18960337 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18960342 | HCID 18960342 | — |
Reaction Steps
An amount of 1.1 g (3.36 mmol) of 3-methoxy-4-tert.-butoxycarbonyloxy-benzaldehyde diethylacetal was dissolved in 40 ml of dried toluene. After the addition of 0.82 g (6.71 mmol) of phenylethanol and 16 mg of potassium hydrogen sulfate, the resulting mixture was stirred for 2 hours under reflux. The ethanol formed was then distilled off slowly, while more, toluene was added to the mixture. After complete removal of the ethanol, the mixture was cooled down and the potassium hydrogen sulfate was filtered off. The filtrate was concentrated in a rotary evaporator. This gave a yellowish, viscous oil, which was dried on an oil pump.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05356752 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-20f9f7fb42344091a7053721bc83cb38 |
| Source note | uspto-grants-1994_10 |