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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425941Generated: October 31, 2026

Sodium Chloride → 5-(2-Cyanobutanoyl)thiophene-2-carbohydrazide

https://huagongshe.com/reaction/2425941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantMethyl 5-(2-cyanobutanoyl)thiophene-2-carboxylateHCID 67087195—
SolventMethanolHCID 887—
Product5-(2-Cyanobutanoyl)thiophene-2-carbohydrazideHCID 67087378—

Reaction Steps

Methyl 5-(2-cyanobutyryl)thiophene-2-carboxylate (213 mg, 0.90 mmol) in methanol was stirred with 0.1 M potassium hydroxide in methanol (9.0 mL, 0.90 mmol) at room temperature for 10 minutes and then with hydrazine monohydrate (225 mg, 4.50 mg) at 80° C. for 6 hours. After addition of saturated aqueous sodium chloride, the reaction solution was extracted with ethyl acetate, dried over anhydrous magnesium sulfate and concentrated to give the crude desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968542B2
Source datasetuspto-grants-2011_06
ORD IDord-9b5ebb64dfaa4e4ea0cc52ddc7ad69e1
Source noteuspto-grants-2011_06