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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351411Generated: October 25, 2026

Tetrahydrofuran → 2-Butyramido-5-chlorobenzamide

https://huagongshe.com/reaction/351411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantButyryl chlorideHCID 8855—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-5-chlorobenzamideHCID 78876—
SolventEthyl AcetateHCID 8857—
Product2-Butyramido-5-chlorobenzamideHCID 21088226—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-5-chlorobenzamide (1.10 g, 6.5 mmol, 1 eq.), 1.000 N NaOH (6.50 mL, 6.5 mmol, 1 eq.) and THF (20 mL) were mixed and stirred at 0° C. To this mixture was added butyryl chloride dropwise (0.68 mL, 6.50 mmol, 1 eq.). More acid chloride and base were added to drive reaction to completion. The reaction was allowed to warm to rt. After 4 days the reaction was worked up by adding ethyl acetate, washing with 1 N HCl (3×), saturated sodium bicarbonate (1×), and brine (1×). The organic layer was dried and stripped to yield 1.44 g of a white powder as product. LCMS detects (M+H)+=241.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183270B2
Source datasetuspto-grants-2007_02
ORD IDord-ca406a373050475d8dfdff6ea911caab
Source noteuspto-grants-2007_02