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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025129Generated: October 30, 2026

Boron Trichloride → HCID 59275511, compound

https://huagongshe.com/reaction/1025129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 59275437HCID 59275437—
SolventDichloromethaneHCID 6344—
ProductHCID 59275511HCID 59275511—

Reaction Steps

To a mixture of 2-(4-fluorophenyl)-5-isopropoxy-N-methyl-6-nitrobenzofuran-3-carboxamide (210.5 mg, 0.565 mmol) in CH2Cl2 (14 mL) at 0° C. under N2 was added trichloroborane (1.70 mL, 1.7 mmol) (1M solution in CH2Cl2). The mixture was then stirred at r.t. for 17 hr. The mixture was evaporated. The reddish orange residue was added 7 ml H2O, and then 3.5 ml 1N HCl, and left standing until the solid turned yellow. The yellow solid product was then filtered and washed with 3×3 ml H2O and dried (182 mg, 93%). 1H NMR (500 MHz, DMSO-d6) δ 10.18 (broad s, 1 H), 8.53 (m, 1 H), 8.31 (s, 1 H), 7.98 (apparent dd, J=8.85, 5.49, 2 H), 7.43 (apparent t, J=8.85, 2 H), 7.28 (s, 1 H,), 2.84 (appeared as d, J=4.58, 3 H). LC/MS were performed by using Shimadzu-VP instrument with UV detection at 220 nm and Waters Micromass. HPLC method: Solvent A=10% MeOH-90% H2O-0.1% TFA, Solvent B=90% MeOH-10% H2O-0.1% TFA, Start % B=0, Final % B=100, Gradient time=2 min, Stop time=3 min, Flow Rate=4 ml/min, Column: Xterra MS 7 um, C18, 3.0×50 mm; (ES+) m/z (M+H)+=331.21, HPLC Rt=1.442 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722688B2
Source datasetuspto-grants-2014_05
ORD IDord-468def686cb44e1f9e6a2d3e59558a4d
Source noteuspto-grants-2014_05