HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426281Generated: November 1, 2026
Perchloric Acid → 3-((tert-Butyldiphenylsilyl)oxy)cyclobutanone
https://huagongshe.com/reaction/1426281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Tert-butyl{[3-(methylsulfinyl)-3-(methylthio)cyclobutyl]oxy}diphenylsilane | HCID 86666495 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-((tert-Butyldiphenylsilyl)oxy)cyclobutanone | HCID 66824505 | 59% |
Reaction Steps
A solution of tert-butyl{[3-(methylsulfinyl)-3-(methylthio)cyclobutyl]oxy}diphenylsilane (17.05 g, 40.7 mmol, from Step 2) in ether (350 mL) cooled to 0° C. was treated with a solution of 6M perchloric acid in water (10 mL) that was pre-diluted with water (7 mL). The bath was removed and stirred overnight. The mixture was poured into pH 7 buffer, and the product was extracted with diethyl ether. The combined extracts were dried over sodium sulfate, decanted and concentrated. The reaction was performed again on the same scale and the two batches were combined for purification. Flash chromatography, eluting with a gradient from 0-5% ethyl acetate/hexanes afforded desired product (15.7 g, 59%). 1H NMR (300 MHz, CDCl3): δ 7.75-7.62 (m, 4H), 7.49-7.33 (m, 6H), 4.59 (tt, 1H), 3.22-3.03 (m, 4H), 1.07 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08933085B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-2c446867334f4a09acf74ea295a4e3c9 |
|---|
| Source note | uspto-grants-2015_01 |
|---|