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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629101Generated: October 30, 2026

Oxalyl chloride → HCID 89907782, compound

https://huagongshe.com/reaction/629101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Trifluoromethoxy)anilineHCID 600848—
Reactant3-Bromo-2-fluorobenzoic acidHCID 2736313—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 89907782HCID 89907782—

Reaction Steps

A solution of oxalyl chloride (0.657 mL, 7.50 mmol) in DCM (10 mL) and of DMF (0.01 mL) were added to a suspension of 3-bromo-2-fluorobenzoic acid (1.095 g, 5 mmol) in DCM (10 mL) and the RM was stirred for at RT for 2 h. The solvent was evaporated off under reduced pressure. The residue was dissolved in DCE (10 mL), treated dropwise with a solution of 4-(trifluoromethoxy)aniline (0.744 mL, 5.50 mmol) and DIPEA (1.747 mL, 10.00 mmol) and the RM was stirred for at RT for 1 h. The RM was treated with an aq. NaHCO3 and extracted with DCM. The combined extracts were washed with water, dried over Na2SO4 and the solvent was evaporated off under reduced pressure to give the crude product which was purified by flash chromatography (Silica gel column, 100 g, n-hexane/EtOAc 2:1) to afford the title compound as beige crystals. UPLC-MS (Condition 2) tR=1.22 min, m/z=375.9/378.0 [M−H−]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315489B2
Source datasetuspto-grants-2016_04
ORD IDord-ea288e1de56544f49a1dbdc7c2c1e38c
Source noteuspto-grants-2016_04