HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2387708Erstellt: 24. Oktober 2026
Trimethylsilylacetylene → Methyl-(3-trimethylsilanylethynyl-benzyl)-carbamic acid tert-butyl ester
https://huagongshe.com/de/reaction/2387708
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | tert-Butyl 3-bromobenzyl(methyl)carbamate | HCID 20738487 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | Methyl-(3-trimethylsilanylethynyl-benzyl)-carbamic acid tert-butyl ester | HCID 60133802 | — |
Reaktionsschritte
TMS-Acetylene (2.2 mL, 15.0 mmol) was added dropwise to commercially available tert-butyl 3-bromobenzyl(methyl)carbamate (3.0 g, 10 mmol), CuI (100 mg, 0.5 mmol) and palladium dichlorobistriphenylphosphine (210 mg, 0.3 mmol) in triethylamine (30 mL) at room temperature under a nitrogen atmosphere. The reaction mixture was heated to 70° C. for 12 hrs before cooling to room temperature and evaporating in vacuo. The residue was triturated with diethyl ether (30 mL), filtered and the filtrate evaporated in vacuo and purified by column chromatography (5% ethyl acetate in hexane) to yield A314.1 (3.2 g, 100%) as a brown oil. HPLC YMC S-5 4.6×33 mm (2 min grad): retention time 2.34 min, M+Na+=340.34
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08268855B2 |
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| Quelldatensatz | uspto-grants-2012_09 |
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| ORD ID | ord-013b702c91bc4f508c0d68b0df41921e |
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| Quellennotiz | uspto-grants-2012_09 |
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