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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820295Generated: November 1, 2026

Acetic Acid → 4-[2-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]ethyl]morpholine

https://huagongshe.com/reaction/1820295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMorpholineHCID 8083—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]acetaldehydeHCID 23109890—
Solvent1,2-DichloroethaneHCID 11—
SolventChloroformHCID 6212—
Product4-[2-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]ethyl]morpholineHCID 57427861138.6%

Reaction Steps

After adding sodium triacetoxyborohydride (0.63 g, 2.98 mmol) to a solution of 1-[1-[2-(tert-butyldiphenylsiloxy)ethyl]cyclohexyl]acetaldehyde (1.29 g, ca. 1.97 mmol), morpholine (0.26 mL, 2.98 mmol) and acetic acid (0.23 mL, 4.02 mmol) in 1,2-dichloroethane (5 mL), the mixture was stirred at room temperature for 2.5 hours. Saturated aqueous sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with chloroform. The organic layer was washed with saturated brine and dried (anhydrous sodium sulfate), and then the solvent was distilled off under reduced pressure to obtain the title compound as a brown oil (1.31 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-cc7dbf41685c4c70aec1e9bf7d085201
Source noteuspto-grants-2009_10