HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-Chloromethyl-5,6,7-trimethoxynaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Hydroxymethyl-5,6,7-trimethoxynaphthalene | HCID 21891578 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Chloromethyl-5,6,7-trimethoxynaphthalene | HCID 21891642 | — |
Reaction Steps
2-Hydroxymethyl-5,6,7-trimethoxynaphthalene (781 mg) was dissolved in chloroform (6 mL), and thionyl chloride (561 mL) was added dropwise to the solution. After stirring at room temperature for 5 hours, the reaction mixture was poured into ice water, and sodium hydrogencarbonate was added to adjust the pH of the reaction mixture to 8 to conduct extraction with ethyl acetate. The resultant organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135473B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-55f8372451644e1b8dd629ed599d8b66 |
| Source note | uspto-grants-2006_11 |