HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40304Generated: October 26, 2026
Methyl iodide → HCID 57691376, compound
https://huagongshe.com/reaction/40304
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Tert-butyl 2-(3-methoxyquinolin-6-yl)acetate | HCID 59843087 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57691376 | HCID 57691376 | — |
Reaction Steps
To a flame-dry 100 ml 3-neck round-bottomed flask was added lithium bis(trimethylsilyl)amide, 1.0 m solution in tetrahydrofuran (5 ml, 5 mmol) and THF (20 mL). The mixture was cooled to −78° C. followed by adding tert-butyl 2-(3-methoxyquinolin-6-yl)acetate (0.88 g, 3 mmol) in THF (10 mL)dropwise via addition funnel. After stirring at −78° C. for 30 min, iodomethane (0.4 ml, 6 mmol) was added. The reaction mixture was stirred for 30 min at −78° C. then allowed to warm to rt and stir for 1 h. The mixture was then quenched with sat. NH4Cl (3 mL). Solvent was removed. The residue was partitioned between EtOAc/water. The organic layer was washed with brine, dried over MgSO4 and removed solvent. The crude material was purified using SiO2 chromatography (Teledyne Isco RediSep®, P/N 68-2203-027, 40 g SiO2, solvent system: hexane:acetone=90%:10%, Flow=30 mL/min) to afford a final product as yellowish liquid. MS m/z: 288.4 (M+H). Calc'd. for C17H21NO3—287.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524900B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-9fe49d7250de4beeba7e7660e2ae2063 |
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| Source note | uspto-grants-2013_09 |
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