戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2387708作成日:2026年10月24日

Trimethylsilylacetylene → Methyl-(3-trimethylsilanylethynyl-benzyl)-carbamic acid tert-butyl ester

https://huagongshe.com/ja/reaction/2387708

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilylacetyleneHCID 66111—
反応物tert-Butyl 3-bromobenzyl(methyl)carbamateHCID 20738487—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒TriethylamineHCID 8471—
生成物Methyl-(3-trimethylsilanylethynyl-benzyl)-carbamic acid tert-butyl esterHCID 60133802—

反応条件

温度70 °C

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08268855B2
出典データセットuspto-grants-2012_09
ORD IDord-013b702c91bc4f508c0d68b0df41921e
出典メモuspto-grants-2012_09