HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351755Generated: October 25, 2026
Nitric Acid → 6-Nitro-2,3-dihydro-1H-indene-1-carboxylic acid
https://huagongshe.com/reaction/351755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 1H-Indene-1-carboxylic acid, 2,3-dihydro- | HCID 85728 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Nitro-2,3-dihydro-1H-indene-1-carboxylic acid | HCID 12318488 | 112.1% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743808B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-ed26aca75b4e42e790aa3e628323a803 |
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| Source note | uspto-grants-2004_06 |
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