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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222604Generated: October 26, 2026

Sodium Hydroxide → Methyl 4-hydrazinyl-3-methylbenzoate

https://huagongshe.com/reaction/222604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantStannous chloride dihydrateHCID 61436—
ReactantMethyl 4-amino-3-methylbenzoateHCID 2736799—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductMethyl 4-hydrazinyl-3-methylbenzoateHCID 59255931—

Reaction Conditions

Temperature-15 °C

Reaction Steps

50 ml of conc. hydrochloric acid are added to methyl 4-amino-3-methylbenzoate (10 g, 61 mmol) and the mixture is cooled down to −15° C. A solution of sodium nitrite (6.3 g, 91 mmol) in 50 ml of water is added dropwise in such a way that the temperature does not exceed −5° C. After stirring at −10° C. for 4 h, a solution of tin(II) chloride dihydrate in 50 ml of conc. hydrochloric acid is added dropwise to the suspension, with the reaction temperature not exceeding −5° C. The viscous suspension is stirred at RT for 15 h before it is adjusted to pH 14 with 200 ml of sodium hydroxide solution (10 N). The reaction mixture is filtered through kieselguhr and Extrelut® (60 g) and rinsed with 2 l of chloroform. The organic phase which is obtained is washed with water (2×200 ml), dried over sodium sulphate and evaporated in vacuo. The residue is stirred up with 120 ml of petroleum ether and filtered. Yield: 6.3 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207349B2
Source datasetuspto-grants-2012_06
ORD IDord-2187742b18c349f082375daad76c1765
Source noteuspto-grants-2012_06