HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606815Generated: October 31, 2026
Triethylamine → N-(2-Fluoro-5-trimethylsilanylethynylbenzyl)-methanesulfonamide
https://huagongshe.com/reaction/606815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | N-(5-bromo-2-fluorobenzyl)methanesulfonamide | HCID 40161431 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-Fluoro-5-trimethylsilanylethynylbenzyl)-methanesulfonamide | HCID 67047541 | 74% |
Reaction Steps
Dissolve zinc (II) bromide (313 mg, 1.20 mmol) in tetrahydrofuran (2.5 mL) and treat with triethylamine (0.64 mL, 4.80 mmol). After 4 min add N-(5-bromo-2-fluorobenzyl)methanesulfonamide (282 mg, 1.00 mmol), (prepared as described in PREPARATION 35), trimethylsilylacetylene (0.30 mL, 2.12 mmol), and tetrakis(triphenylphosphine)palladium (0) (58 mg, 0.050 mmol) to the reddish solution. Heat to 60° C. in a sealed tube overnight, cool to room temperature and filter through diatomaceous earth with ethyl acetate. Concentrate the filtrate and purify the residue by silica gel chromatography, eluting with 75:25 hexanes:ethyl acetate, to give the title compound as a white crystalline solid (220 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915424B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-d2f92a028c4849448d327706acd8e3fe |
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| Source note | uspto-grants-2011_03 |
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