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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1457363Erstellt: 26. Oktober 2026

Water → 3-(2-Bromopropanoyl)spiro[benzo[e][1,3]oxazine-2,1'-cyclohexan]-4(3H)-one

https://huagongshe.com/reaction/1457363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPyridineHCID 1049—
EduktPropanoyl bromide, 2-bromo-HCID 79047—
Eduktspiro[benzo[e][1,3]oxazine-2,1'-cyclohexan]-4(3H)-oneHCID 652743—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(2-Bromopropanoyl)spiro[benzo[e][1,3]oxazine-2,1'-cyclohexan]-4(3H)-oneHCID 10338052—

Reaktionsschritte

A solution of 89.1 ml of 2-bromopropionyl bromide in 95 ml of methylene chloride and a solution of 61.13 g of pyridine in 95 ml of methylene chloride are added dropwise to a suspension of 140 g of spiro[2,3-dihydro-4H-1,3-benzoxazine-2,1'-cyclohexan]-4-one in 190 ml of methylene chloride under nitrogen atmosphere at -5° C. during about 45 minutes. Then the mixture is stirred at a room temperature for 6 hours. The reaction mixture is poured into 500 ml of water and the mixture is extracted with methylene chloride. The extract is washed, dried and evaporated to remove the solvent and the residue obtained is crystallized from methanol and the crystals are collected by filtration to obtain 197.3 g of 3-(2-bromopropionyl)-spiro[2,3-dihydro-4H-1,3-benzoxazine-2,1'-cyclohexan]-4-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05847115
Quelldatensatzuspto-grants-1998_12
ORD IDord-37c4039c7465403c8b81d4b3d0260745
Quellennotizuspto-grants-1998_12