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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952639Generated: November 4, 2026

Triethylamine → 3-Bromo-5-(3-hydroxy-benzylcarbamoyl)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1952639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-(Aminomethyl)phenolHCID 735894—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 68226869HCID 68226869—
SolventDimethylformamideHCID 6228—
Product3-Bromo-5-(3-hydroxy-benzylcarbamoyl)-thiophene-2-carboxylic acid methyl esterHCID 6822668159%

Reaction Steps

To a solution of 3-Bromo-thiophene-2,5-dicarboxylic acid 2-methyl ester (204 mg, 0.76 mmol) in anhydrous DMF (7 mL) was added triethylamine (0.32 mL, 2.28 mmol), HBTU (0.43 g, 1.14 mmol), HOBT (123 mg, 0.91 mmol), and 3-Aminomethyl-phenol (110 mg, 0.91 mmol). The mixture was stirred at room temperature 15 h, then quenched by pouring into EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash chromatography with 0-50% EtOAc in hexane to afford the desired product (0.1647 g, 59% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404859B2
Source datasetuspto-grants-2013_03
ORD IDord-fb5e29d296cc48b99d1bad5d6e7be0ec
Source noteuspto-grants-2013_03