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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128558Generated: October 27, 2026

Tetrahydrofuran → 2-Fluoro-4-chloro-5cyclopentyloxyphenylhydrazine

https://huagongshe.com/reaction/128558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium HydroxideHCID 14797—
ReactantTin dichloride dihydrateHCID 43835034—
Reactant2-Fluoro-4-chloro-5-cyclopentyloxyphenyl-diazonium fluoroborateHCID 88265160—
SolventHydrochloric AcidHCID 313—
Product2-Fluoro-4-chloro-5cyclopentyloxyphenylhydrazineHCID 1527939690.9%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of tin (II) chloride monohydrate (200 g, 0.886 mol) dissolved in concentrated hydrochloric acid (200 ml) and THF (200 ml) was added a THF (200 ml) solution of 2-fluoro-4-chloro-5-cyclopentyloxyphenyl-diazonium fluoroborate (31.3 g, 0.094 mol) under cooling at 0 to 5° C. After stirring for 8 hours at that temperature, an aqueous solution (1,000 ml) of potassium hydroxide (160 g) was added thereto. The solid that was formed was separated by filtration, and the filtrate was extracted with ethyl acetate (1,000 ml×3). The extract was washed with a saturated aqueous solution of sodium chloride (1,000 ml), and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and the solvent was distilled off under reduced pressure to obtain 2-fluoro-4-chloro-5cyclopentyloxyphenylhydrazine as brown crystals (20.9 g, 85.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464811
Source datasetuspto-grants-1995_11
ORD IDord-4ab8b71a92be4d498ff145d0edc0c967
Source noteuspto-grants-1995_11