Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Product | HCID 240120 | HCID 240120 | 172.1% |
Reaction Steps
In a 100-ml three-necked flask, 24 g (0.2 mole) of phenylacetaldehyde, 18 g (0.24 mole) of n-butanol, 10 g of anhydrous magnesium sulfate and 0.1 mg of stannous chloride dihydrate were charged. The resulting mixture was stirred at 100° C. under atmospheric pressure for 6 hours in a nitrogen atmosphere. After the removal of magnesium sulfate, the residue was purified by chromatography on a silica gel column to give 43.1 g of phenylacetaldehyde dibutyl acetal [R1 =a benzyl group, R2 =a hydrogen atom and R3 =an n-butyl group] (yield: 86.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05792876 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-5bad6e3c18e44b40903a35a086ddbabc |
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| Source note | uspto-grants-1998_08 |
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