Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347422Generated: October 30, 2026

Tetrabutylammonium Fluoride → HCID 69244301, compound

https://huagongshe.com/reaction/347422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantTert-butyl 4-[cis-3-(tert-butyldiphenylsilanyloxy)cyclohexyl]-2,2-dimethylbutyrateHCID 69241608—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69244301HCID 69244301—

Reaction Conditions

Temperature60 °C

Reaction Steps

2 g of tert-butyl 4-[cis-3-(tert-butyl-diphenylsilanyloxy)cyclohexyl]-2,2-dimethylbutyrate are dissolved in 10 ml of tetrahydrofuran, and 8 ml of a 1 M solution of tetrabutylammonium fluoride and tetrahydrofuran are added. The mixture is stirred at 60° C. for 2 hours. The reaction mixture is concentrated under reduced pressure and purified on silica gel using the mobile phase n-heptane:ethyl acetate=20:1=>1:1. This gives 730 mg of tert-butyl 4-[cis-3-hydroxycyclohexyl)-2,2-dimethylbutyrate as an oil. C16H30O3 (270.42), Rf(n-heptane:ethyl acetate=5:1)=0.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173151B2
Source datasetuspto-grants-2007_02
ORD IDord-8ac0bfc15c5144e28c19bb52c7e56ac5
Source noteuspto-grants-2007_02