Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20408Generated: October 26, 2026

Tetrabutylammonium Fluoride → HCID 68561911, compound

https://huagongshe.com/reaction/20408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant1,3-Difluoro-5-(2-nitroethyl)benzeneHCID 55250753—
Reactant(2R,5R)-2-(2,2-Dimethylpropoxy)-5-formylmorpholine-4-carboxylic acid tert-butyl esterHCID 86615359—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68561911HCID 6856191134%

Reaction Steps

Add tetrabutylammonium fluoride (18.32 mL, 18.32 mmol, 1.0 M in tetrahydrofuran) to (2R,5R)-2-(2,2-dimethylpropoxy)-5-formylmorpholine-4-carboxylic acid tert-butyl ester (5.02 g, 16.66 mmol) and 1,3-difluoro-5-(2-nitroethyl)-benzene (3.43 g, 18.32 mmol) in tetrahydrofuran (28 mL) at −10° C. and stir 20 minutes. Pour into ice cold saturated aqueous sodium chloride and extract with ethyl acetate. Wash with 0.1 N aqueous citric acid and saturated aqueous sodium chloride, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 20:80 to 30%:70 diethyl ether:hexanes) to give a mixture of 2 diastereomers (3.66 g, 75:25 mixture) which are separated using chiral chromatography to give the desired compound (˜2.45 g, 34.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745438B2
Source datasetuspto-grants-2010_06
ORD IDord-be30b5997f8b4be99dee6c5b4bacce7b
Source noteuspto-grants-2010_06