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HRID 560951作成日:2026年10月25日

11-Bromoundecanoic acid → N3(CH2)10C(O)Cl

https://huagongshe.com/reaction/560951

反応式

関与物質

役割名称HCID仕込み量
反応物11-Bromoundecanoic acidHCID 17812—
反応物Sodium AzideHCID 33557—
反応物Oxalyl chlorideHCID 65578—
反応物11-Azidoundecanoic acidHCID 454094—
溶媒BenzeneHCID 241—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物N3(CH2)10C(O)ClHCID 22283452—

反応条件

温度80 °C

反応手順

In a glass reaction vessel, 10.6 grams (40 mmol) of 11-Bromoundecanoic acid was dissolved in 225 milliliters DMF and 26 grams (400 mmol) sodium azide was added. The resulting stirred mixture was heated to 80° C. for 16 h, and then the reaction mixture was worked up with ether and brine. The ether layer was dried (MgSO4), filtered, and concentrated to 9.5 grams of N3(CH2)10C(O)OH as a pale yellow oil which was used without purification. In a glass reaction vessel, the N3(CH2)10C(O)OH was dissolved in 120 milliliters benzene and 12.7 grams (100 mmol) oxalyl chloride was added. The reaction was allowed to stir for 20 h, at which time the volatiles were removed in vacuo. The resulting residue was dissolved in pentane and filtered in a nitrogen atmosphere to remove solids. Concentration of the filtrate afforded N3(CH2)10C(O)Cl as a clear, yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063164B2
出典データセットuspto-grants-2011_11
ORD IDord-1517c54aba0f452892d62f89cf8b329f
出典メモuspto-grants-2011_11