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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086735Generated: October 31, 2026

Trimethylsilyl iodide → HCID 178525614, compound

https://huagongshe.com/reaction/1086735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 178496220HCID 178496220—
SolventDichloromethaneHCID 6344—
ProductHCID 178525614HCID 17852561429%

Reaction Steps

3-{1-[(cis-4-Carboxy-cyclohexyl)carbamoyl]-cyclopentyl}-2-[2-(methoxy)ethoxymethyl]propanoic acid (0.80 g, 2 mmole) was dissolved in dry dichloromethane (15 ml) and treated with trimethylsilyl iodide (1.4 ml, 10 mmole) at 0° C. under nitrogen. After 6 hours at 0° C., the reaction was poured into ice-cold dilute sodium hydrogen carbonate and washed with dichloromethane. The aqueous phase was acidified with concentrated hydrochloric acid and extracted with ethyl acetate (3×50 ml). The first extract contained starting material, the second and third extracts were combined, washed with dilute sodium thiosulphate, dried (Na2SO4) and evaporated to give an orange oil. The residue was azeotroped with dichloromethane and washed with dichloromethane to give the title compound as a glassy foam (0.22 g, 29%). Found: C,57.24; H,8.07; N,3.42. C19H31NO7. 0.1 CH2Cl2 0.25 H2O requires C,57.58; H,8.02; N,3.52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030654
Source datasetuspto-grants-1991_07
ORD IDord-1010dcc61c6e4037a9ce88e50309d1fe
Source noteuspto-grants-1991_07