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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107812Generated: November 1, 2026

1-Fluoro-2-nitrobenzene → HCID 14625401, compound

https://huagongshe.com/reaction/2107812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 23046774HCID 23046774—
SolventDimethylformamideHCID 6228—
ProductHCID 14625401HCID 14625401—

Reaction Steps

A mixture of hexahydro-5-phenyl-1H-1,2,5-triazepine dihydrochloride (15.0 g), 1-fluoro-2-nitrobenzene (9.84 ml), N,N-diisopropylethylamine (36.5 ml) in N,N-dimethylformamide (150 ml) was magnetically stirred and heated at 75°-80° for 5 hours under nitrogen. The solution was evaporated under oil pump vacuum and the residual syrup was mixed with chloroform and dilute sodium hydroxide. The aqueous phase was extracted once more with chloroform and the combined chloroform extracts were dried (MgSO4). The solution was evaporated to a syrup which was subjected to an oil pump vacuum. This material in benzene was applied to a column (80×4.0 cm) of dry column grade neutral alumina (Woelm) prepacked in benzene. Elution was with benzene and monitoring of fractions was by t.l.c. on Alox 25 uv254 plates (Brinkmann) with benzene as developer. The fractions containing the major component were evaporated to a syrup which was crystallized from benzeneheptane; wt. 13.82 g (78%), mp=118°-120°. Recrystallization from benzeneheptane gave pure titled product, mp=119° -121°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935515
Source datasetuspto-grants-1990_06
ORD IDord-1d4b9e27136d4ea09d103c14d05912bc
Source noteuspto-grants-1990_06