Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639232Generated: October 25, 2026

Sulfuric Acid → 2-(4-Ethoxyphenyl)-2-methyl-2-silapropanol

https://huagongshe.com/reaction/1639232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Ethoxyphenyl)-2-methyl-2-silapropyl acetateHCID 14014483—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-(4-Ethoxyphenyl)-2-methyl-2-silapropanolHCID 1353234486.4%

Reaction Steps

To 48 mL of a lM diethyl ether solution of lithium aluminum hydride (1.82 g, 0.048 mole) that had been cooled to 0° C. was added dropwise a solution of 11.0 g (0.044 mole) of 2-(4-ethoxyphenyl)-2-methyl-2-silapropyl acetate in 50 mL of diethyl ether. Fifteen minutes after the addition was complete, the reaction mixture was allowed to warm to room temperature, and it was stirred for 4.5 hours. To the reaction mixture were then added sequentially 1.8 mL of water, 1.8 mL of an aqueous 15% solution of sodium hydroxide, and 5.4 mL of water. Sufficient aqueous 10% sulfuric acid was added to dissolve the undissolved salts, and this mixture was extracted twice with diethyl ether. The combined extracts were washed with water and then with a saturated aqueous sodium carbonate solution that had been diluted with water (50:50). After being dried over anhydrous potassium carbonate and filtered, the solvent was evaporated under reduced pressure, leaving 8.0 g of 2-(4-ethoxyphenyl)-2-methyl-2-silapropanol as an orange oil. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04883789
Source datasetuspto-grants-1989_11
ORD IDord-7a084f13d8174e34bac1e049a0e9bd3f
Source noteuspto-grants-1989_11