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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367787Generated: October 31, 2026

Chlorotrimethylsilane → Ethanone, 2-bromo-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-

https://huagongshe.com/reaction/1367787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTetrahydrofuranHCID 8028—
ReactantBromineHCID 24408—
ReactantSodium hexamethyidisilazaneHCID 45051731—
ReactantHCID 66936654HCID 66936654—
ProductEthanone, 2-bromo-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-HCID 11150315—

Reaction Steps

To the product of step (b) (23.4 g, 0.113 mol) in 600 mL of THF at −78° C. was added 135 mL of 1.0 M sodium hexamethyldisilazane in THF (Sigma-Aldrich). After 1 hour, trimethylsilyl chloride (15.8 mL, 0.124 mol) was added. After another 30 minutes, bromine (5.82 mL, 0.113 mol) was added. After 10 minutes, the reaction was quenched by diluting the reaction mixture with diethyl ether and pouring it onto 500 mL of 5% aqueous Na2SO3 premixed with 500 mL of 5% aqueous NaHCO3. The phases were separated and the organic phase was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give the title compound as an oil that solidified upon storage in the freezer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893256B2
Source datasetuspto-grants-2011_02
ORD IDord-bc5959c128c5449080888c0c886daa74
Source noteuspto-grants-2011_02