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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820294Generated: October 31, 2026

Tempo → 1-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]acetaldehyde

https://huagongshe.com/reaction/1820294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTempoHCID 2724126—
ReactantIodo benzene diacetateHCID 12217721—
Reactant2-[1-(2-tert-Butyldiphenylsiloxyethyl)cyclohexyl]ethanolHCID 57427860—
SolventDichloromethaneHCID 6344—
Product1-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]acetaldehydeHCID 23109890160.2%

Reaction Steps

After adding 2,2,6,6-tetramethylpiperidine 1-oxyl free radical (31 mg, 0.20 mmol) to a solution of 2-[1-[2-(tert-butyldiphenylsiloxy)ethyl]cyclohexyl]ethanol (810 mg, 1.97 mmol) and iodobenzene diacetate (700 mg, 2.17 mmol) in methylene chloride (10 mL), the mixture was stirred at room temperature for 4 hours. The reaction mixture was washed with saturated aqueous sodium hydrogencarbonate and saturated brine in that order and dried (anhydrous sodium sulfate), and then the solvent was distilled off under reduced pressure to obtain the title compound as a brown oil (1.29 g). This was used without purification for the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601843B2
Source datasetuspto-grants-2009_10
ORD IDord-e72eb954a3f44f64b8ee325944ed2115
Source noteuspto-grants-2009_10