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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239887Generated: November 1, 2026

Tributylamine → HCID 86618521, compound

https://huagongshe.com/reaction/2239887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium ChlorideHCID 25517—
Reactantethyl 2-(3-chlorophenyl)-2-oxoacetateHCID 2758814—
CatalystTitanium TetrachlorideHCID 24193—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86618521HCID 86618521—

Reaction Steps

To a flask was added ethyl 2-(3-chlorophenyl)-2-oxoacetate (1.8 g, 8.47 mmol) and acetic anhydride (1.60 ml, 16.93 mmol) in DCE (5 ml) at RT. To the resulting solution was added titanium(IV) chloride (16.93 ml, 16.93 mmol) and tributylamine (2.42 ml, 10.16 mmol). The solution was heated to reflux for 12 hours. The solution was then cooled in ice, and a solution of ammonium chloride was added. The mixture was stirred for 30 min. LC/MS indicated all starting material was gone. The solution was washed with 1×NH4Cl, 1N HCl, water, dried and concentrated in vacuo to provide 3-(3-chlorophenyl)furan-2,5-dione which was used as is in the next reaction. LC/MS, m/e 209 (M+1). HPLC Rt, 2.89 min. Waters Sunfire C18 column (4.6×50 mm). 0%-100% B. Solvent B: (90% MeOH, 10% H2O, 0.1% TFA). Solvent A: (10% MeOH, 90% H2O, 0.1% TFA). Gradient, start % B=0, final % B=100, gradient time 4 min. hold at 100% B 1 min, flow rate 4 mL/min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723336B2
Source datasetuspto-grants-2010_05
ORD IDord-bcc4d356e4914ac38c1ce5bab8aa2622
Source noteuspto-grants-2010_05