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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093717Generated: November 1, 2026

Boron tribromide → HCID 56847984, compound

https://huagongshe.com/reaction/2093717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 56847982HCID 56847982—
SolventDichloromethaneHCID 6344—
ProductHCID 56847984HCID 5684798452%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 220 mg (0.54 mmol) N-[(3-fluorophenyl)-methyl]-2-(methoxymethyl)-4-methyl-7-(trifluoromethyl)-quinoline-3-carboxylic acid amide (Example 15) in DCM (5 ml) was cooled to −78° C. and 5.4 ml (5.4 mmol, 2M in DCM) boron tribromide was added. After heating to 0° C., the mixture was stirred for 16 h at this temperature. Quenching was then carried out with a 1M aq. NaHCO3 sol. (15 ml) and a 10%-strength aq. Na2S2O3 sol. It was then diluted with MeOH and DCM and the organic phase was separated, dried over MgSO4 and concentrated in a vacuum. After CC (EtOAc/hexane 1:1→EtOAc/DCM 1:1) of the residue, 110 mg (0.28 mmol, 52%) N-[(3-fluorophenyl)-methyl]-2-(hydroxy-methyl)-4-methyl-7-(trifluoromethyl)-quinoline-3-carboxylic acid amide (example 17) was obtained. MS: m/z 393.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445512B2
Source datasetuspto-grants-2013_05
ORD IDord-1afe871badfe4010826d69a7be3955a2
Source noteuspto-grants-2013_05