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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922299Generated: October 30, 2026

Hexamethyldisilazane → HCID 57835929, compound

https://huagongshe.com/reaction/922299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
Reactant4-HydroxybenzophenoneHCID 14347—
ReactantEthyl trimethylsilylacetateHCID 77687—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57835929HCID 5783592955.9%

Reaction Steps

To a solution of HMDS (21.17 g, 131.1 mmol) in THF (200 mL) was cooled to −40° C. Then it was added with n-BuLi (56.7 mL, 136.22 mmol) and stirred at same temperature for 45 min. After that (4-hydroxyphenyl)(phenyl)methanone (2 g, 10 mmol) in THF was added slowly over a period of 10 min and stirred at −40° C. to −30° C. for one hour. Then Ethyl(trimethylsilyl)acetate (2.42 g, 15.1 mmol) was added drop wise and stirred at 0° C. to 15° C. for completion of starting material (4 h). After reaction completed reaction was quenched with ammonium chloride and then THF was evaporated under vacuum and the resulted solution was partitioned between water and Ethyl acetate. The combined organic layer was dried and evaporated to get crude. The crude was purified through chromatography and triturated with n-Hexane to afford red color oil as product (1.5 g, Yield: 55.9%); 1H NMR (300 MHz, CDCl3): δ 7.31-7.33 (m, 4H), 7.01-7.74 (d, 1H), 6.7-7.16 (m, 4H), 6.25 (s, 1H), 3.94-3.99 (q, 2H), 1.07-1.10 (t, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278915B2
Source datasetuspto-grants-2016_03
ORD IDord-ebe72d0e3866447daeec54fd7603a6f8
Source noteuspto-grants-2016_03