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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364635Generated: October 31, 2026

2-Fluorobenzoyl chloride → 90183-00-9

https://huagongshe.com/reaction/364635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoyl chlorideHCID 9808—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-AminoquinuclidineHCID 123238—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product90183-00-9HCID 2483427664.4%

Reaction Steps

In a closed system, a solution of 3-aminoquinuclidine (2.52 g, 0.020 mole) in 10 ml anhydrous ether was added dropwise to a stirred solution of 2-fluorobenzoyl chloride (3.13 g, 0.020 mole) in 100 ml anhydrous ether. After the addition was complete, the mixture was stirred another hour and the solid product (as the hydrochloride salt) was collected by filtration under nitrogen to give 4.75 g (84%). TLC analysis (3% conc. ammonium hydroxide in methanol) showed the presence of 3-aminoquinuclidine. The salt was dissolved in 10 ml water, basified with 6N sodium hydroxide solution, and extracted three times with 50 ml portions of methylene chloride. The combined extract was dried over magnesium sulfate and concentrated to give 3.67 g of the product as the free base. Recrystallization from tolueneisooctane gave 2.33 g of a white solid (some toluene insoluble material was removed by decanting the hot toluene solution). The solid free base was dissolved in 10 ml methanol, treated with excess ethereal hydrogen chloride and 100 ml isopropyl ether was added. The salt separated from solution as an oil, but crystallized on trituration. The white solid was collected under nitrogen to give 2.60 g; m.p. 233°-234° C. Mass spectrum (E.I.) m/e (% relative intensity): 248 (15), 125 (13), 123 (100), 109 (80), 96 (24), 95 (45), 84 (14), 75 (19), 70 (64), 42 (44), 41 (18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04605652
Source datasetuspto-grants-1986_08
ORD IDord-7291cf0319a74ede9de43e6341612a7d
Source noteuspto-grants-1986_08