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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166219Generated: November 3, 2026

Stannous chloride dihydrate → (5-Chloro-2-methoxyphenyl)hydrazine

https://huagongshe.com/reaction/1166219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
ReactantBenzenediazonium, 5-chloro-2-methoxy-, chloride (1:1)HCID 66730—
Reactant5-Chloro-2-methoxyanilineHCID 66763—
CatalystHCID 16212471HCID 16212471—
SolventHydrochloric AcidHCID 313—
Product(5-Chloro-2-methoxyphenyl)hydrazineHCID 40892684%

Reaction Conditions

Temperature0 °C

Reaction Steps

Tin(II)chloride dihydrate (SnCl2.2H2O, 121 g, 0.54 mol) was dissolved in 300 ml concentrated HCl at −72° C. Diazo Red RC (Azoic Diazo No. 10, C.I. 37120, Fast Red RC Salt, Aldrich Chemical Co., 50 g, 0.18 mole) was added in portions with vigorous mechanical stirring. After the addition was complete, the reaction was stirred at 0° C. for three hours. The tan solid was filtered and washed with concentrated HCl, then stirred for 30 minutes in a mixture of 500 ml of dichloromethane and 500 ml 2N NaOH. The organic layer was separated, dried over sodium sulfate, concentrated under vacuum, and the resulting oil crystallized from 100 ml of diethyl ether to yield (5-chloro-2-methoxyphenyl)hydrazine (26.4 g, 84%). 1H NMR (300 MHz, CDCl3) δ6.96 (1H, d, J=2.4 Hz), 6.70 (1H, dd, 8.4, 2.4 Hz), 6.65 (1H, d, J=8.4 Hz), 3.81 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613786B2
Source datasetuspto-grants-2003_09
ORD IDord-8d18fb50e9d442679598b9ad1e910427
Source noteuspto-grants-2003_09