Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 19840936 | HCID 19840936 | — |
| Product | HCID 19840938 | HCID 19840938 | 35% |
Reaction Steps
Reaction of 4-(1,1-dimethylpropyl)-2-(1-methylethyl)-5-methylphenol (22.02 g, 0.1 mol), which may be prepared as described by W. Koenigs and R. W. Carl, Chem. Ber., (1981) 25, 3892-3903, 40% formaldehyde solution (70 mL, 0.93 mol), p-dioxane (150 mL) and sulfuric acid (10 mL) according to the procedure described in Example 2, provided after chromatography and short-path distillation, 9.18 g (35% yield) of 6-(1,1-dimethylpropyl)-5-methyl-8-(1-methylethyl)-4H-1,3-benzodioxin (GLC purity 98%); 1H-NMR (CDCl3)δ 0.70 (3H, t, J=7 HZ), 1.20 (6H, d, J=7 Hz), 1.35 (6H, s), 1.78 (2H, q, J=7 Hz), 2.15(3H, s), 3.0-3.5 (1H, m), 4.80 (2H, s), 5.17(2H, s), 7.03 (1H, s); IR (film) νmax 2950, 1575, 1470 cm-1 ; MS m/e 262, 233, 217, 203, 175, 161; UVλmax (ethanol) 226 nm (ε=5530), 283 nm (ε=1520).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04880775 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-ef207f217a794ea5b18a01f3015387f8 |
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| Source note | uspto-grants-1989_11 |
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