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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277772Generated: October 31, 2026

Hydrazine hydrate (1:1) → Methyl alpha-methylthio-alpha-(3-chloro-4-aminophenyl)propionate

https://huagongshe.com/reaction/1277772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantMethyl alpha-methylthio-alpha-(3-chloro-4-phthalimidophenyl)propionateHCID 12819454—
SolventMethanolHCID 887—
ProductMethyl alpha-methylthio-alpha-(3-chloro-4-aminophenyl)propionateHCID 1291766692%

Reaction Steps

Methyl α-methylthio-α-(3-chloro-4-phthalimido-phenyl)propionate was suspended in 7 ml of methanol, and 97 mg of hydrazine hydrate was added. The mixture was stirred at room temperature, and then heated under reflux for 1 hour. The mixture was concentrated under reduced pressure, and an aqueous solution of ammonium chloride and methylene chloride were added. The organic layer was separated, and dried over anhydrous sodium sulfate. Concentration under reduced pressure yielded 231 mg of methyl α-methylthio-α-(3-chloro-4-aminophenyl)propionate as a pale yellow oil. Yield 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04278802
Source datasetuspto-grants-1981_07
ORD IDord-4e85efa006ac4317bf37c622da25fff5
Source noteuspto-grants-1981_07