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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298206Generated: October 30, 2026

Methyl 5-bromothiophene-2-carboxylate → 5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/2298206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-bromothiophene-2-carboxylateHCID 605713—
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
CatalystTriethylamineHCID 8471—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl EsterHCID 5407533963,406.199%

Reaction Steps

A mixture of prop-2-ynyl-carbamic Acid tert-butyl ester (1.67 g, 0.011 mmol), 5-bromo-thiophene-2-carboxylic Acid methyl ester (2.50 g, 0.011 mmol), tetrakistriphenylphosphine(0) palladium (0.622 g, 0.0538 mmol), Cul (0.102 g, 0.538 mmol) and triethylamine (1.57 mL, 0.011 mmol) in 50 mL acetonitrile under nitrogen was heated at reflux for 16 h. The reaction was cooled to room temperature, diluted with 75 mL EtOAc, washed with 5.5% HCl, water and brine, dried over MgSO4, filtered and concentrated in vacuo to an oil. The product was purified via flash chromatography (9:1 to 4:1 hexanes:EtOAc) to afford the title compound as an oil (2.06 g). MS 313 (M+18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-55b00b1b75844a65ba12045b406f9060
Source noteuspto-grants-2002_12