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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558646Generated: October 29, 2026

Trimethylsilylacetylene → 5-Ethynylthiophene-2-sulfonamide

https://huagongshe.com/reaction/558646

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 numberUS08063048B2
Source datasetuspto-grants-2011_11
ORD IDord-f981a49da84b4cf5b6cdad4992d0160b
Source noteuspto-grants-2011_11