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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293755Generated: November 2, 2026

Trimethylsilylacetylene → 5-Ethynylthiophene-2-sulfonamide

https://huagongshe.com/reaction/1293755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-Bromo-2-thiophenesulfonamideHCID 1241304—
Product5-Ethynylthiophene-2-sulfonamideHCID 86043795—

Reaction Steps

Prepared from 5-bromo-thiophene-2-sulfonic acid amide (1.94 g, 8 mmol) and trimethylsilylacetylene (2.2 mL, 12 mmol) by applying in analogous manner the procedures described in example D.1 (method 1, steps 1–2). Obtained after chromatographic purification of the crude product (SiO2, 0–75% AcOEt/heptane) as a light brown solid (0.49 g, 33%). MS (ISP) 186.1 [(M−H)−]; mp 114–116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238808B2
Source datasetuspto-grants-2007_07
ORD IDord-1f6620eaf5fb4cec9290219b90a1ae39
Source noteuspto-grants-2007_07