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HRID 553280作成日:2026年10月26日

Tri-o-tolylphosphine → Tert-butyl 2,6-dichlorophenethyl(3-(2-oxopropyl)benzyl)carbamate

https://huagongshe.com/reaction/553280

反応式

関与物質

役割名称HCID仕込み量
反応物Tri-o-tolylphosphineHCID 80271—
反応物Methoxytri-n-butylstannaneHCID 11964040—
反応物1-Acetoxy-3-methyl-1,3-butadieneHCID 53401854—
反応物[2-(2,6-Dichloro-phenyl)-ethyl]-(3-iodo-benzyl)-carbamic acid tert-butyl esterHCID 67165818—
溶媒TolueneHCID 1140—
生成物Tert-butyl 2,6-dichlorophenethyl(3-(2-oxopropyl)benzyl)carbamateHCID 67165764—

反応条件

温度100 °C

反応手順

[2-(2,6-Dichloro-phenyl)-ethyl]-(3-iodo-benzyl)-carbamic acid tert-butyl ester (Example 14, step b) (500 mg), tributyltin methoxide (350 μL), isoprenyl acetate (170 μL), tri-o-tolylphosphine (30 mg) and toluene (20 mL) were charged to a flask and the solution degassed with nitrogen for 5 minutes. Palladium acetate (10 mg) was added and the resultant mixture heated to 100° C., under nitrogen, for 3 hours. On cooling, potassium fluoride (580 mg) in water (3 mL) was added, stir at room temperature for 18 hours. The solids were filtered off, and the filter cake washed with ethyl acetate. The filtrate was evaporated and purified on silica, eluting with a gradient of iso-hexane/ethyl acetate [4:1 to 2:1], to give the subtitle product as an oil (230 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951954B2
出典データセットuspto-grants-2011_05
ORD IDord-ad8f92d1c2294bb6a3c2dd8618b77800
出典メモuspto-grants-2011_05