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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098317Generated: November 2, 2026

Sodium Bicarbonate → 2-Fluoro-6,n,n-trimethyl-3-morpholin-4-ylbenzamide

https://huagongshe.com/reaction/1098317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1,1'-Difluoro-2,2'-bipyridinium Bis(tetrafluoroborate)HCID 2733931—
Reactant2,N,N-Trimethyl-5-morpholin-4-ylbenzamideHCID 23156788—
SolventAcetonitrileHCID 6342—
Product2-Fluoro-6,n,n-trimethyl-3-morpholin-4-ylbenzamideHCID 231567607.2%
Product4-fluoro-2,N,N-trimethyl-5-morpholin-4-ylbenzamideHCID 231568655.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

393 mg (1.10 mmol) of N,N′-difluoro-2,2′-bipyridinium bis(tetrafluoroborate) was added to 7 ml of an acetonitrile solution containing 458 mg (1.84 mmol) of the 2, N,N-trimethyl-5-morpholin-4-ylbenzamide obtained in Step B of Example 80 under cooling on ice. The obtained mixture was stirred at 0° C. for 1 hour, then at a room temperature for 1 hour, then at 50° C. for 1 hour, then at 80° C. for 2.5 days, and then under heating to reflux for 2 hours. Thereafter, 357 mg (1.0 mmol) of N,N′-difluoro-2,2′-bipyridinium bis(tetrafluoroborate) was further added to the reaction solution, and the obtained mixture was further stirred for 20 minutes. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction solution, and the mixture was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and was then concentrated. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:3 to 1:1), so as to obtain 25.8 mg (5.3%) of 4-fluoro-2,N,N-trimethyl-5-morpholin-4-ylbenzamide in the form of an oily substance, and also obtain 35.1 mg (7.2%) of 2-fluoro-6,N,N-trimethyl-3-morpholin-4-ylbenzamide in the form of an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143274B2
Source datasetuspto-grants-2012_03
ORD IDord-fe6ed1284d814452a0c7f1e5510c64a0
Source noteuspto-grants-2012_03