HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356400Generated: October 27, 2026
Methyl iodide → 2-Chloro-n-ethyl-6-(ethyldimethylsilyl)benzamide
https://huagongshe.com/reaction/356400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 2-Chloro-n-ethyl-6-(trimethylsilyl)benzamide | HCID 18630379 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-n-ethyl-6-(ethyldimethylsilyl)benzamide | HCID 18630286 | 46% |
Reaction Steps
To a solution of the compound of example 45 (1.28 g, 5 mmol) and TMEDA (0.91 mL, 6.0 mmol, 1.2 eq) in THF at -78° C. was added a 1.7M solution of t-BuLi in pentane (7.1 mL, 12 mmol, 2.4 eq) such that the temperature was less than -70° C. The reaction was stirred at -78° C. for 2 h and methyl iodide (0.44 mL, 7.0 mmol, 1.4 eq) was added. The reaction was stirred for 15 min at -78° C. and worked up in the usual manner. The crude product was recrystallized from aq methanol and then from hexanes to afford the title compound as white crystals (0.62 g, 46%). m.p. 94°-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834447 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-4ad21b26f4ff4181bc6520c966fed506 |
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| Source note | uspto-grants-1998_11 |
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