Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 255963Erstellt: 25. Oktober 2026

Hydrochloric Acid → 1-(Hexadecyloxy)but-3-EN-2-OL

https://huagongshe.com/reaction/255963

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBromoetheneHCID 11641—
EduktMagnesiumHCID 5462224—
Edukt(Hexadecyloxy) acetaldehydeHCID 14785848—
Katalysator1,1-DibromoethaneHCID 11201—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(Hexadecyloxy)but-3-EN-2-OLHCID 1395907141,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirring mixture of 5.67 g of magnesium in 25 ml of tetrahydrofuran was added 10 drops of dibromoethane as an initiator. After the reaction began another 100 ml of tetrahydrofuran was added followed by the dropwise addition of a solution of 49.85 g of vinyl bromide in 250 ml of tetrahydrofuran at a rate to maintain reflux. After all of the magnesium had reacted, the solution was cooled to 0° C. and a solution of 44.2 g of (hexadecyloxy) acetaldehyde, prepared by the procedure of Example 3, in 175 ml of ether was added dropwise over 1/2 hour. After 1 hour at room temperature dilute hydrochloric acid was added. The tetrahydrofuran was removed and the residue was extracted with ether. The ether layer was washed with brine, dried and the solvent removed. The residue was purified by HPLC [hexane: ether (9:1), two columns, two passes] giving an oil which was distilled via a Kugelrohr apparatus (185°-190° C., 0.2 mm) giving a colorles oil which solidified on standing to give 20.17 g of the desired compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04699990
Quelldatensatzuspto-grants-1987_10
ORD IDord-41414b2cf6584599ac72779c5a79dd96
Quellennotizuspto-grants-1987_10