Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 59756873 | HCID 59756873 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 68993386 | HCID 68993386 | — |
Reaction Steps
(6,7-Dimethoxyquinolin-4-yl)methanol (1.11 g, 5.07 mmol) was dissolved in thionyl chloride (10 mL) at 0° C. The reaction mixture was stirred at 0° C. for 20 minutes then warmed to room temperature and stirred for 3.5 hours. The reaction mixture was diluted with benzene (20 ml) then concentrated under vacuum. The remaining solid was triturated with benzene then dried under high vacuum to afford 1.35 g of 4-(chloromethyl)-6,7-dimethoxyquinoline hydrochloride as a yellow solid. MS (ESI, pos. ion) m/z: 238.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338455B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-2b1162627fa64f17aa9bf5a47e77dcea |
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| Source note | uspto-grants-2012_12 |
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