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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342010Generated: October 26, 2026

Methyl 2-bromobenzoate → Methyl 2-(3-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-oxopropyl)benzoate

https://huagongshe.com/reaction/342010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-bromobenzoateHCID 11894—
ReactantLithium ChlorideHCID 433294—
Reactant1-(3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl)-2-propen-1-olHCID 53406285—
Reactantlithium acetateHCID 178506943—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(3-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-oxopropyl)benzoateHCID 5339488192.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A degassed suspension of 1-(3-(2-(7-chloro-2-quinolinyl)ethenyl)phenyl)-2-propen-1-ol (Example 80, Step 1, 50.30 g, 156 mmol), LiOAc/2H2O (41.2 g, 404 mmol), LiCl (6.84 g, 161 mmol), Pd(OAc)2 (1.00 g, 4.45 mmol) and methyl 2-bromobenzoate (33.5 g, 156 mmol) in 300 mL of DMF was stirred at 95° C. for 4 h. The mixture was cooled to r.t (room temperature) and added to 1.8 L of water. The product was extracted with hot EtOAc, dried over Na2SO4 and concentrated. It was dissolved in toluene and filtered through silica with toluene. Recrystallization in 1.2 L of EtOAc:hexanes 1:1 afforded 65.57 g of the title compound. Recrystallization of the mother liquors in 400 mL EtOAc:hexanes 1:3 afforded a further 8.30 g (86% overall yield) of the title material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856322
Source datasetuspto-grants-1999_01
ORD IDord-aafc7411f8f24fdc861a6e77a88da586
Source noteuspto-grants-1999_01