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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272172Generated: October 30, 2026

Diisopropylethylamine → HCID 58486771, compound

https://huagongshe.com/reaction/2272172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
ReactantHCID 58487378HCID 58487378—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethanolHCID 887—
SolventLithium HydroxideHCID 3939—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58486771HCID 5848677166.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under an atmosphere of argon, 2,6-difluorobenzoyl chloride (8.6 mg, 48 μmol) was added to a stirred solution of 15 (9.5 mg, 32 μmol), Hünig's base (17 μL, 13 mg, 97 μmol), and DMAP (1 mg, 8 μmol) in dichloromethane (200 μL) at room temperature. The reaction was stirred for 25 min. The solution was diluted with tetrahydrofuran (750 μL), methanol (500 μL) and 1.2 M lithium hydroxide solution (250 μL). The mixture was stirred and heated to 60° C. for 10 min then cooled to room temperature and diluted with dichloromethane (5 mL) and dried with sodium sulfate. The mixture was concentrated under reduced pressure. Flash chromatography (ISCO system, silica, 0-50% ethyl acetate in hexane) provided 16 (9.3 mg, 66%) as a solid: LRESIMS m/z 434.0 [M+H]+, calcd. for C18H11Br1F2N3O3 434.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-66ce00b15dab454f83074c965f676405
Source noteuspto-grants-2015_09