HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351411Generated: October 25, 2026
Tetrahydrofuran → 2-Butyramido-5-chlorobenzamide
https://huagongshe.com/reaction/351411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Amino-5-chlorobenzamide | HCID 78876 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Butyramido-5-chlorobenzamide | HCID 21088226 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183270B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-ca406a373050475d8dfdff6ea911caab |
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| Source note | uspto-grants-2007_02 |
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