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HRID 241087Erstellt: 25. Oktober 2026

Hydrochloric Acid → 7-Bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride

https://huagongshe.com/reaction/241087

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
Edukt1,4-DioxaneHCID 31275—
Edukttert-Butyl 7-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylateHCID 25220760—
LösungsmittelDiethyl EtherHCID 3283—
Produkt7-Bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochlorideHCID 6682013798%

Reaktionsschritte

1,1-dimethylethyl 7-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (10 g, 30.5 mmol) was taken into hot ethanol (10 mL) followed by addition of 4 M hydrogen chloride in dioxane solution (2.1 eq, 16 mL) and the resulting solution was allowed to slowly cool to ambient temperature over one hour. An excess of ethyl ether was then added and the resulting slurry was filtered. The filter cake was washed with ethyl ether and dried to give 7-bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride (7.9 g, 98% yield) as a colorless crystalline solid. MS (EI) for C9H10NOBr: 229 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08648066B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-236090125a054c49b7aaa8c573f5deca
Quellennotizuspto-grants-2014_02