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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukttert-Butyl 3-bromobenzyl(methyl)carbamateHCID 20738487—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelTriethylamineHCID 8471—
ProduktMethyl-(3-trimethylsilanylethynyl-benzyl)-carbamic acid tert-butyl esterHCID 60133802—

Reaktionsbedingungen

Temperatur70 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08268855B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-013b702c91bc4f508c0d68b0df41921e
Quellennotizuspto-grants-2012_09