HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418309Generated: October 30, 2026
Phosphorus oxychloride → 6-Methoxy-1-methyl-3,4-dihydro-2-naphthaldehyde
https://huagongshe.com/reaction/418309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 7-methoxy-4-methyl-1,2-dihydronaphthalene | HCID 11829938 | — |
| Product | 6-Methoxy-1-methyl-3,4-dihydro-2-naphthaldehyde | HCID 13694442 | 44% |
Reaction Steps
To a solution of Compound B (0.44 g, 2.5 mmole) in dry dimethylfomamide (1.3 ml, 16.8 mmole) at ice cooling and stirring under argon atmosphere, phosphorus oxychloride (0.62 ml, 6.65 mmole) was added drop-by-drop in 2 minutes. The reaction mixture was stirred in an oil bath of 70-75° C. for 3 hours. After cooling in an ice bath, ice (6 g) was added, then sodium acetate (anhydrous, 3.7 g) was added, and the mixture (pH 6) was warmed in an oil bath at 70-75° C. for 15 minutes. After cooling, it was extracted with ether (1×10 ml and 3×5 ml), the combined organic solutions were washed with water (3×3 ml), dried (magnesium sulfate), decolorized (with activated carbon), and evaporated. The residue (0.33 g) was recrystallized from cyclohexane (2 ml) and dried over potassium hydroxide in a vacuum giving the pure product 6-Methoxy-1-methyl-3,4-dihydro-2-naphthaldehyde (Compound C, 0.22 g, 44%) as light brown crystals, mp. 70-72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093269B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e27d3c73318d4401975197eb1a2b4c77 |
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| Source note | uspto-grants-2012_01 |
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