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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162955Generated: October 29, 2026

Sodium hydride → HCID 57558159, compound

https://huagongshe.com/reaction/1162955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,3-Dioxan-5-ol, 2-phenyl-HCID 74362—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
SolventDimethylformamideHCID 6228—
ProductHCID 57558159HCID 5755815961%

Reaction Steps

Sodium hydride (133 mg, 3.32 mmol) was added to 5 mL of a solution of cis-1,3-O-benzylideneglycerol (300 mg, 1.66 mmol) in DMF, and the mixture was stirred at room temperature for two hours. (2-bromoethoxy)-tert-butyldimethylsilane (534 μl, 3.32 mmol) was added to the mixture which was then stirred at room temperature for two hours. Aqueous saturated ammonium chloride was added to the mixture, followed by extraction with ethyl acetate. The extract was washed with saturated saline and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain a crude product, tert-butyldimethyl-[2-(2-phenyl-[1,3]dioxan-5-yloxy)ethoxy]silane (343 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820693B2
Source datasetuspto-grants-2010_10
ORD IDord-6f8e057bb5d3400f99a5216b22f6d7c3
Source noteuspto-grants-2010_10