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HRID 1635662Erstellt: 26. Oktober 2026

2,4,4,6-Tetrabromocyclohexa-2,5-dienone → methyl (2S)-1-(6-bromo-1,3-benzoxazol-2-yl)-2-piperidinecarboxylate

https://huagongshe.com/reaction/1635662

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,4,6-Tetrabromocyclohexa-2,5-dienoneHCID 88433—
Eduktmethyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylateHCID 10220819—
LösungsmittelDichloromethaneHCID 6344—
Produktmethyl (2S)-1-(6-bromo-1,3-benzoxazol-2-yl)-2-piperidinecarboxylateHCID 994977195,1%

Reaktionsschritte

2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one (4.7 g) was added to a solution of methyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylate (3.0 g) [see Preparation 2] in dichloromethane (60 ml) at −10° C. over a period of 10 mins. The reaction mixture was then warmed to room temperature and diluted with dichloromethane. The organic layer was washed with saturated sodium hydrogen carbonate, then with 1N sodium hydroxide solution, dried over sodium sulphate and the solvent removed under reduced pressure to afford methyl (2S)-1-(6-bromo-1,3-benzoxazol-2-yl)-2-piperidinecarboxylate (3.7 g) as a purple coloured oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06509464B1
Quelldatensatzuspto-grants-2003_01
ORD IDord-6bcf47333ff34cbf9b1f4f50a2a24175
Quellennotizuspto-grants-2003_01