tert-Butyldimethylsilyl chloride → Tert-butyl(3-ethoxy-2,2-dimethylpropoxy)dimethylsilane

Reaction equation

[CH3:1][C:2]([CH3:9])([CH2:5][O:6][CH2:7][CH3:8])[CH2:3][OH:4].[Si:10](Cl)([C:13]([CH3:16])([CH3:15])[CH3:14])([CH3:12])[CH3:11]>>[CH3:1][C:2]([CH3:9])([CH2:3][O:4][Si:10]([C:13]([CH3:16])([CH3:15])[CH3:14])([CH3:12])[CH3:11])[CH2:5][O:6][CH2:7][CH3:8]

Participants

Reactant 2

HCID 28928tert-Butyldimethylsilyl chloride

HCID 126982853-Ethoxy-2,2-dimethylpropan-1-ol

Product 1

HCID 23090613Tert-butyl(3-ethoxy-2,2-dimethylpropoxy)dimethylsilane

Procedure

According to the procedure as described in Example 3,2,2-dimethyl-1-ethoxy-3-[(tert-butyldimethylsilyl)oxy]propane was prepared from intermediate 2,2-dimethyl-3-ethoxy-1-propanol and reagent tert-butyidimethylsilyl chloride.

Sources & evidence

ORD record: ord-9a9448b7764049e9bfb09776de261208
Source dataset: uspto-grants-2008_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07399812B2

Reaction notes

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