Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394825Generated: October 28, 2026

Citric Acid → HCID 18630071, compound

https://huagongshe.com/reaction/2394825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDiethylamineHCID 8021—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCyclohexaneHCID 8078—
Reactant3-Fluorobenzoic AcidHCID 9968—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantN,N-diethyl-3-fluorobenzamideHCID 963334—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18630071HCID 1863007181%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1.3M s-BuLi in cyclohexane (7.7 mL, 0.01 mol) was added dropwise to THF (30 mL) and TMEDA (1.28 g, 0.011 mol) cooled to -78° C. under nitrogen with stirring. To this mixture was added 0.0097 mol of N,N-diethyl-3-fluorobenzamide (prepared from 3-fluorobenzoic acid and diethylamine according to the procedures of the examples of b and f) dissolved in a minimum amount of THF dropwise. The mixture was stirred for 10 min and injected with t-butyldimethylsilylchloride (3.01 g, 0.02 mol). The reaction mixture was stirred and warmed to RT overnight. 25% citric acid (15 mL) was added and the mixture was extracted three times with ether. The ether extracts were combined and washed twice with water, dried (MgSO4), concentrated, and purified by RC eluting with 7:15 ethyl acetate/hexanes. The title compound was recovered as a tan solid in 81% yield. m.p. 50°-51° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811411
Source datasetuspto-grants-1998_09
ORD IDord-e6cb3d33bc9d403498955bd58e230e09
Source noteuspto-grants-1998_09