HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062583Generated: November 2, 2026
Methyl chloroformate → 6-Methoxy-2-(3-methoxyphenyl)quinoline
https://huagongshe.com/reaction/1062583
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 6-Methoxyquinoline N-oxide | HCID 253821 | — |
| Reactant | HCID 178490745 | HCID 178490745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methoxy-2-(3-methoxyphenyl)quinoline | HCID 22064610 | 46.4% |
Reaction Steps
To a solution of 6-methoxyquinoline-N-oxide (175 mg, 1.0 mmol) in THF (3 mL) at room temperature is added methyl chloroformate (77 uL, 1.0 mmol). The mixture is cooled to 0° C. and 3-methoxyphenylmagnesium bromide (2 mL of 1M, 2 mmol) is added dropwise. The mixture is stirred for 16 h while warming to room temperature. The solvent is removed in vacuo and the resulting residue is partitioned between water and CH2Cl2. The organic phase is washed with water and brine, dried over MgSO4, filtered and concentrated. Flash chromotography (0-20% EtOAc/hexanes) yields 6-methoxy-2-(3-methoxy-phenyl)-quinoline (123 mg, 46% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06962928B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-1d146646474d4e82b4f9e4f5c4ba3f89 |
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| Source note | uspto-grants-2005_11 |
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