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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374100Erstellt: 25. Oktober 2026

1,3,3-Trimethyl-2-methyleneindoline → HCID 19360917, Verbindung

https://huagongshe.com/reaction/374100

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3,3-Trimethyl-2-methyleneindolineHCID 8351—
Edukt3-Hydroxymethyl-1-nitroso-2-naphtholHCID 23286284—
LösungsmittelEthanolHCID 702—
ProduktHCID 19360917HCID 1936091720,9%

Reaktionsschritte

In 100 ml of ethanol, 7.0 g (40 mmol) of 1,3,3-trimethyl-2-methyleneindoline and 8.0 g (40 mmol) of 3-hydroxymethyl-1-nitroso-2-naphthol were dissolved and the solution was heated to reflux for 3 hours. After removal of the solvent, purification was conducted by column chromatography and recrystallization from hexane to obtain 3.0 g of 1,3,3-trimethyl-5'-hydroxymethylspiro [indoline-2,3'-[3H]-naphtho[2,1-b](1,4)oxazine] as a white solid. In 50 ml of methylene dichloride, 1.1 g (3 mmol) of the thus obtained spirooxazine compound was dissolved and 4 ml of triethylamine was added thereto, and then 0.5 g (5 mmol) of methacrylic acid chloride was added dropwise thereto at room temperature and the mixture was allowed to react. After removal of solvent, purification was conducted by column chromatography and recrystallization from hexane to obtain 1.0 g of 1,3,3-trimethyl-5'-methacryloxymethylspiro[indoline-2,3'-[3H]-naphtho[2,1 -b](1,4)oxazine] as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166345
Quelldatensatzuspto-grants-1992_11
ORD IDord-f8c33322f814485f8f784f215173855e
Quellennotizuspto-grants-1992_11