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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806998Generated: October 26, 2026

Water → 5-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentan-1-ol

https://huagongshe.com/reaction/1806998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
Reactant3,3-Dimethylpentane-1,5-diolHCID 12810774—
SolventDimethylformamideHCID 6228—
Product5-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentan-1-olHCID 866404199.4%

Reaction Steps

Step A To the solution of 3,3-dimethyl-pentane-1,5-diol (1.5 g, 11 mmol) prepared in Example 116a Step A. in anhydrous dimethylformamide (15 mL) was added NaH (60%, 0.68 g, 17 mmol). The mixture was stirred at room temperature for 15 min, then (2-bromoethoxy)-tert-butyldimethylsilane (3.3 g, 14 mmol) was added. The mixture was stirred at room temperature for 1 h. Water was added. The mixture was extracted with ethyl acetate twice. The combined organic layers were washed with brine, dried over MgSO4, and concentrated. The residue was purified by chromatography (EtOAc:hexanes=1:3) to give 5-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentan-1-ol as a yellow oil (0.3 g, 9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-b9aa0463f9cc443dbb855f4fdacdd276
Source noteuspto-grants-2013_01