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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1297573Erstellt: 25. Oktober 2026

Sulfuric Acid → Di-tert-amylcyclohexylphosphine

https://huagongshe.com/reaction/1297573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktChlorocyclohexaneHCID 10952—
EduktMagnesiumHCID 5462224—
EduktDi-tert-amylphosphinous chlorideHCID 23032008—
KatalysatorCuprous chlorideHCID 62652—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDi-tert-amylcyclohexylphosphineHCID 2292548196,7%

Reaktionsschritte

In a 300 ml four-necked flask thoroughly purged with nitrogen, 10.4 g (0.05 mol) of di-tert-amylphosphinous chloride, 0.10 g (0.001 mol (corresponding to 2% by mol)) of copper(I) chloride and 30 ml of tetrahydrofuran were placed. To the contents of the flask, a Grignard reagent solution previously prepared from 8.3 g (0.060 mol) of cyclohexyl chloride and 2.0 g (0.08 mol) of metallic magnesium in 50 ml of tetrahydrofuran was dropwise added over a period of 1 hour with maintaining the temperature at 25° C. to 30° C. After the dropwise addition was completed, stirring was conducted at a temperature of 35° C. to 40° C. for 6 hours. After the temperature of the reaction solution was returned to room temperature, 20 ml of toluene and 20 ml of a 5% sulfuric acid aqueous solution were added to the reaction solution to perform liquid separation. Then, the organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent and a low-boiling component were distilled off under reduced pressure to obtain 12.4 g (purity: 94.9%) of the aimed di-tert-amylcyclohexylphosphine as an oily substance. The yield was 90.2%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07250535B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-b131fcae618b4d9db60a8b5908619afd
Quellennotizuspto-grants-2007_07