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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639005Generated: October 31, 2026

1-Fluoro-2-nitrobenzene → HCID 14625404, compound

https://huagongshe.com/reaction/1639005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 23046778HCID 23046778—
SolventDimethylformamideHCID 6228—
ProductHCID 14625404HCID 14625404—

Reaction Steps

A mixture of hexahydro-5-(phenylmethyl)-1H-1,2,5-triazepine dihydrochloride (35.0 g), 1-fluoro-2-nitrobenzene (21 ml), N,N-diisopropylethylamine (81 ml) in N,N-dimethylformamide (400 ml) was stirred and heated at 75°-80° (under reflux) under ntirogen for 5 hours. The solution was evaporated to a syrup under oil pump vacuum and the residue was mixed with chloroform and dilute sodium hydroxide. The aqueous phase was extracted several times with chloroform. The combined extracts were dried (MgSO4) and evaporated to a syrup wich was subjected to an oil pump vacuum. The syrup in toluene was applied to a column (94×8.7 cm) of dry column grade neutral alumina prepacked in toluene. Elution with toluene removed a faster moving yellow impurity. Fractions were monitored by t.l.c. on Alox-25 uv254 plates (Brinkmann) with chloroform as developer. As soon as the major component started to issue the eluting solvent was changed to toluene-chloroform (4:1), toluene-chloroform (1:1) and finally chloroform. Appropriate fractions were evaporated to a syrup which was crystallized from ether-heptane; wt. 35.7 g (86%), mp=90°-92°. Recrystallization from chloroform-ether-heptane gave pure titled product, mp=90°-92°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882323
Source datasetuspto-grants-1989_11
ORD IDord-7a40a454b72c4485b290ef572709d9fa
Source noteuspto-grants-1989_11