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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508531Generated: October 31, 2026

Stannous chloride dihydrate → (3-Fluoro-4-methoxyphenyl)hydrazine--hydrogen chloride (1/1)

https://huagongshe.com/reaction/1508531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant3-Fluoro-4-methoxyanilineHCID 581110—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product(3-Fluoro-4-methoxyphenyl)hydrazine--hydrogen chloride (1/1)HCID 44203039—

Reaction Steps

A suspension of 3-fluoro-4-methoxyaniline (1.5871 g, 11.24 mmol) in hydrochloric acid, 37% (14 ml) was diazotized with sodium nitrite (0.776 g, 11.24 mmol) in water (7 mL) and reduced with tin(ii) chloride dihydrate (1.873 mL, 22.49 mmol) in hydrochloric acid, 37% (5 ml) at 0° C. The reaction was then stirred for 20 min at room temperature. The precipitate was collected by filtration. The cake was triturated with ethanol (50 mL, room temp) followed by filtration to give a pale yellow solid as the titled compound. 1H NMR (DMSO-d6, 500 MHz) δ 10.17 (br s, 2H), 8.12 (br s, 1H), 7.10 (dd, J=9.0, 9.0 Hz, 1H), 6.96 (dd, J=13.0, 2.5 Hz, 1H), 6.80-6.76 (m, 1H) 3.76 (s, 3H), 3.42 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221834B2
Source datasetuspto-grants-2015_12
ORD IDord-eaeb877c5a0f41bd95cb8b7f5b9dcc29
Source noteuspto-grants-2015_12