HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922299Generated: October 30, 2026
Hexamethyldisilazane → HCID 57835929, compound
https://huagongshe.com/reaction/922299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Reactant | Ethyl trimethylsilylacetate | HCID 77687 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57835929 | HCID 57835929 | 55.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278915B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-ebe72d0e3866447daeec54fd7603a6f8 |
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| Source note | uspto-grants-2016_03 |
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