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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351755Erstellt: 26. Oktober 2026

Nitric Acid → 6-Nitro-2,3-dihydro-1H-indene-1-carboxylic acid

https://huagongshe.com/reaction/351755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
Edukt1H-Indene-1-carboxylic acid, 2,3-dihydro-HCID 85728—
LösungsmittelSulfuric AcidHCID 1118—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-Nitro-2,3-dihydro-1H-indene-1-carboxylic acidHCID 12318488112,1%

Reaktionsschritte

A solution of 1-indancarboxylic acid (30 g), prepared according to the method of Hansen et al. Helv. Chim. Acta 1982, 33, 325-343, in dichloromethane (50 ml) was mixed with concentrated sulphuric acid (300 ml) at −10° C. A mixture of 100% HNO3 (11.4 g) in concentrated H2SO4 (96 ml) was added dropwise under vigorous stirring below −10° C. After stirring for one hour at 10° C., the mixture was poured onto ice. Extraction with ethyl acetate (2×300 ml), drying (anh. MgSO4) and finally evaporation of the organic solvent afforded 42 g of the title compound. Mp: 126-130° C. 5-Nitro-3-benzothiophencarboxylic acid was prepared from 3-bromo-5-nitrobenzothiophene via the corresponding 3-cyanobenzothiophene derivative according to EP Pat. No. 88-301073 (CA110(9):75203y (1988), J. Amer. Chem. Soc. 1948, 70, 1955, and J. Chem. Soc.(c) 1967, 1899.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743808B1
Quelldatensatzuspto-grants-2004_06
ORD IDord-ed26aca75b4e42e790aa3e628323a803
Quellennotizuspto-grants-2004_06