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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTert-butyl-(2,3-difluoro-benzyloxy)-dimethyl-silaneHCID 18549933—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl-(2,3-difluoro-4-methyl-benzyloxy)-dimethyl-silaneHCID 18550272105.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548526B2
Source datasetuspto-grants-2003_04
ORD IDord-f63d948ab7ad442c8ab7a8222616fa85
Source noteuspto-grants-2003_04