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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252199Generated: October 30, 2026

3-(Trifluoromethyl)benzoyl chloride → HCID 59860299, compound

https://huagongshe.com/reaction/252199

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
ReactantHCID 59860296HCID 59860296—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 59860299HCID 59860299—

Reaction Steps

To a solution of 4-chloro-11-oxa-7,10-diaza-benzo[b]fluoren-1-ylamine (35 mg, 0.13 mmol) in the dichloromethane (2.0 mL) is added 3-(trifluoromethyl)benzoyl chloride (54.2 mg, 0.26 mmol). After the mixture is stirred for 24 hours at room temperature, it is diluted with EtOAc and washed with saturated K2CO3, brine and water. The organic layer is dried, filtered and concentrated to give crude product, which is purified by flash silica gel column eluting with CH2Cl2 (100%) gradient to CH2Cl2/MeOH (98/2) to give the product as a solid: 1H NMR 400 MHz (DMSO) δ 10.85 (s, 1H), 9.53 (s, 1H), 9.37 (s, 1H), 8.63 (d, 1H), 8.24 (s, 1H), 8.19 (d, 1H), 7.87 (d, 1H), 7.77 (d, 1H), 7.72 (d, 1H), 7.67 (t, 1H), 7.48 (d, 1H); MS m/z 442.85 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868018B2
Source datasetuspto-grants-2011_01
ORD IDord-0df4a5fc0d924b02b9f2d96a21e71cfc
Source noteuspto-grants-2011_01