HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266362Generated: October 27, 2026
Methyl iodide → Tert-butyl-(2,3-difluoro-4-methyl-benzyloxy)-dimethyl-silane
https://huagongshe.com/reaction/1266362
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Tert-butyl-(2,3-difluoro-benzyloxy)-dimethyl-silane | HCID 18549933 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl-(2,3-difluoro-4-methyl-benzyloxy)-dimethyl-silane | HCID 18550272 | 105.3% |
Reaction Steps
To a solution of TMEDA (3.9 mL, 3.0 g, 26 mmol) in THF (33 mL) at −78° C. was added sec butyllithium (20 mL, 1.3 M in hexane, 26 mmol). After stirring for 20 minutes, a solution of tert-butyl-(2,3-difluoro-benzyloxy)-dimethyl-silane (6.0 g, 23 mmol) in 17 mL of THF was added dropwise. After stirring for 1 hour, the solution was added dropwise to a solution of methyl iodide (8 mL) in THF (40 mL) at −20° C. After stirring for 18 hours, the mixture was quenched with saturated aqueous NH4Cl, extracted 3× into ether, and the combined organic layers were dried over MgSO4, filtered and concentrated in vacuo, giving 6.6 g of tert-butyl-(2,3-difluoro-4-methyl-benzyloxy)-dimethyl-silane as a light yellow oil. 1H NMR (400 MHz, CDCl3) δ 7.07 (app. t, 1H, J=7.2 Hz), 6.89 (app. t, 1H, J=7.3 Hz), 4.74 (s, 2H), 2.26 (d, 3H, J=1.9 Hz), 0.87 (s, 9H), 0.07 (s, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548526B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-f63d948ab7ad442c8ab7a8222616fa85 |
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| Source note | uspto-grants-2003_04 |
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