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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 560951생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/560951

반응식

참여 물질

역할이름HCID투입량
반응물11-Bromoundecanoic acidHCID 17812—
반응물Sodium AzideHCID 33557—
반응물Oxalyl chlorideHCID 65578—
반응물11-Azidoundecanoic acidHCID 454094—
용매BenzeneHCID 241—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물N3(CH2)10C(O)ClHCID 22283452—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063164B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-1517c54aba0f452892d62f89cf8b329f
출처 메모uspto-grants-2011_11