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HRID 542140Erstellt: 26. Oktober 2026

Diisopropylamine → HCID 178469142, Verbindung

https://huagongshe.com/reaction/542140

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktPropanoic acid, 2,2,3,3,3-pentafluoro-, ethyl esterHCID 67928—
EduktLithium diisopropylamideHCID 2724682—
EduktButyllithiumHCID 178418339—
EduktHCID 178472209HCID 178472209—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 178469142HCID 17846914230,7%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

To a -78° C. solution of LDA (0.10 mol), prepared from 0.10 mol of n-BuLi and 14 ml (0.10 mol) of diisopropylamine in 70 ml ether was added a solution of 10.0 g (0.042 mol) of product of Example 34 in 20 ml of ether slowly to maintain a temperature below -60° C. After stirring for 30 minutes, the reaction mixture was treated with 21 ml (0.042 mol) of ethyl pentafluoropropionate. After stirring at -78° C. for 15 minutes, the reaction mixture was warmed to 10° C. in 0.5 hour and poured into 100 ml of water, and extracted with ether. The ether extract was extracted with 10% K2CO3. The combined aqueous layer and K2CO3 extract was acidified with concentrated HCl to give 4.73 g (29.5%) of beige solid; mp 115°-117° C. (dec). A 2.73 g (0.00709 mol) of the solid was heated in a kugelrohr pot at 130° C. for 0.5 hour. The distillate and residue were combined and dissolved in ether. The ether solution was dried (CaSO4) and concentrated to give 2.0 g (76.9%) of product as a solid; mp 36°-38° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04655816
Quelldatensatzuspto-grants-1987_04
ORD IDord-b132052dda1a42b084f6d6e2749934bd
Quellennotizuspto-grants-1987_04