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HRID 879950作成日:2026年10月25日

Undecylenic Acid → 1-Undecene, 11-fluoro-

https://huagongshe.com/reaction/879950

反応式

関与物質

役割名称HCID仕込み量
反応物Undecylenic AcidHCID 5634—
反応物2,2,2-TrifluoroethanolHCID 6409—
反応物Myristyl bromideHCID 8208—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物10-Undecynoic acidHCID 31039—
反応物2,2,2-trifluoroethyl Undec-10-enoateHCID 11482501—
反応物2,2,2-Trifluoroethyl undec-10-ynoateHCID 86658304—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Dimethyl SulfoxideHCID 679—
生成物1-Undecene, 11-fluoro-HCID 68046—

反応手順

Glassware used for surface modification was cleaned with organic solvents and etched overnight in basic detergent solution. Prior to use, it was rinsed with ultrapure water and dried at 120° C. 1-Hexadecene (98%, Sigma-Aldrich) was purified by column chromatography and vacuum distillation. 1-Hexadecyne was obtained by reacting 1-bromotetradecane with lithium acetylide ethylenediamine complex in dimethylsulfoxide. 11-Fluoroundec-1-ene was synthesized as described elsewhere.14 2,2,2-Trifluoroethyl undec-10-ynoate and 2,2,2-trifluoroethyl undec-10-enoate were synthesized by esterification of 10-undecynoic acid, respectively 10-undecenoic acid, with 2,2,2-trifluoroethanol using N,N′-dicyclohexylcarbodiimide as a coupling reagent and 4-dimethylaminopyridine as a catalyst. Solvents used were either of analytical grade or distilled prior to use.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993479B2
出典データセットuspto-grants-2015_03
ORD IDord-0b2f3dd8dcb24da89fa6a77c85fd4e20
出典メモuspto-grants-2015_03