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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261475Generated: November 2, 2026

Nitric Acid → 2,3-Dihydro-1'-acetyl-5-nitrospiro[benzofuran-2,4'-piperidine]

https://huagongshe.com/reaction/261475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantWaterHCID 962—
Reactant2,3-Dihydro-1'-acetylspiro[benzofuran-2,4'-piperidine]HCID 12733234—
SolventAcetic AcidHCID 176—
Product2,3-Dihydro-1'-acetyl-5-nitrospiro[benzofuran-2,4'-piperidine]HCID 12733235—

Reaction Conditions

Temperature100 °C

Reaction Steps

3.8 g of nitric acid (sp gr 1.42) in 30 ml of glacial acetic acid is added dropwise to a stirred solution of 4.7 g of 2,3-dihydro-1'-acetylspiro[benzofuran-2,4'-piperidine] in 65 ml of glacial acetic acid. After total addition, the reaction mixture is slowly heated to 100° C. over a 2 hour span and then cooled and poured into 500 ml of water. The diluted mixture is extracted with chloroform and the chloroform extracts are washed sequentially with a saturated sodium bicarbonate solution, a saturated sodium chloride solution and then dried. The chloroform is removed under reduced pressure. The residue is triturated with ether causing an orange precipitate, which is collected and recrystallized first from an ethyl alcohol-ether mixture and then from ethyl alcohol to provide the product, 2,3-dihydro-1'-acetyl-5-nitrospiro[benzofuran-2,4'-piperidine], mp 149°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166120
Source datasetuspto-grants-1979_08
ORD IDord-962b27478bb0484a82381b574ac38ac4
Source noteuspto-grants-1979_08