Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phenoxyethanol | HCID 31236 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 18960338 | HCID 18960338 | — |
| Product | HCID 18960339 | HCID 18960339 | — |
Reaction Steps
A mixture of 2 g (7.45 mmol) of 4-(tert.-butoxycarbonyloxy)-benzaldehyde dimethylacetal, 2.06 g (14.9 mmol) of 2-phenoxyethanol and 40 mg of potassium hydrogensulfate was heated to the boil in 30 ml of dried toluene under a reflux condenser. After heating for 1 hour, the methanol formed was distilled off slowly, while more toluene was added to the mixture. After complete removal of the methanol, the mixture was cooled down, the potassium hydrogen sulfate catalyst was filtered off and the toluene was stripped off. The oily residue was dissolved in dichloromethane and washed with water. The organic phase was dried over magnesium sulfate. After the solvent had been stripped off under reduced pressure, the product was dried in an oil pump vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05356752 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-9ff583a7b94347ae89c9dbccde130a47 |
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| Source note | uspto-grants-1994_10 |
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