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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerchloric AcidHCID 24247—
ReactantTert-butyl{[3-(methylsulfinyl)-3-(methylthio)cyclobutyl]oxy}diphenylsilaneHCID 86666495—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3-((tert-Butyldiphenylsilyl)oxy)cyclobutanoneHCID 6682450559%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933085B2
Source datasetuspto-grants-2015_01
ORD IDord-2c446867334f4a09acf74ea295a4e3c9
Source noteuspto-grants-2015_01