HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3,4-Dimethoxynaphthalene-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1,2-dimethoxynaphthalene | HCID 299257 | — |
| Solvent | 1,4-Dichlorobenzene | HCID 4685 | — |
| Product | 3,4-Dimethoxynaphthalene-1-carbaldehyde | HCID 13495554 | 68.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A mixture of 1,2-dimethoxynaphthalene (0.74 g, 4 mmol) and DMF (0.8 mL, 10 mmol) in dichlorobenzene (0.8 mL) was stirred with POCl3 at 100° C. for 2 h. The reaction mixture was cooled to 0° C., quenched with a cold aqueous solution of NaOAc, diluted with H2O and extracted with benzene. The extracts were dried (MgSO4), concentrated and in vacuo and dichlorobenzene was removed by kugelrohr distillation at 110° C./0.5 mm Hg. Column chromatography (20% EtOAc in hexane) gave the product 18 (596 mg, 68%), which was used in the following step without further purification. 1H NMR (CDCl3) 10.42 (s, 1H), 9.00-9.15 (m, 1H), 8.15-8.30 (m, 1H), 7.61 (s, 1H), 7.50-7.65 (m, 2H), 4.12 (s, 3H), 4.07 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253207B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-01cbff267cff485bb284840083c2a36e |
| Source note | uspto-grants-2007_08 |