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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040593Generated: October 29, 2026

Stannous Chloride → (4-(4-Cyclopentyl-3-(trifluoromethyl)benzyloxy)phenyl)hydrazine Hydrochloride

https://huagongshe.com/reaction/2040593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
ReactantSodium NitriteHCID 23668193—
Reactant4-(4-Cyclopentyl-3-(trifluoromethyl)benzyloxy)aniline hydrochlorideHCID 67211154—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product(4-(4-Cyclopentyl-3-(trifluoromethyl)benzyloxy)phenyl)hydrazine HydrochlorideHCID 67211930129.6%

Reaction Conditions

Temperature-1 °C

Reaction Steps

4-(4-Cyclopentyl-3-(trifluoromethyl)benzyloxy)aniline hydrochloride (30 g, 81 mmol) was suspended in water (285 mL), and concentrated HCl (18 mL) was added. The suspension was stirred efficiently and cooled in ice/IPA bath to −0° C. Sodium nitrite (5.57 g, 81 mmol) in water (12 mL) was added. After addition, the reaction was stirred at 2° C. for 40 minutes. Some solids on the side were washed with ACN (10 mL). The mixture was cooled to −1° C. and tin (II)chloride (45.9 g, 242 mmol) dissolved in concentrated HCl (30 mL) was added slowly. A thick precipitate was formed and stirring was continued for 30 minutes. The mixture was warmed to room temperature and stirred for 3 h. The mixture was filtered, washed with HCl (0.1 M) and the solid was dried under vacuum to give the title compound (40.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580841B2
Source datasetuspto-grants-2013_11
ORD IDord-f68fffd89f4c4b17876632ee9a91a9ec
Source noteuspto-grants-2013_11