HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400368Generated: October 31, 2026
Potassium Carbonate → 4-chloro-N-(5-phenyl-1,3,4-thiadiazol-2-yl)butanamide
https://huagongshe.com/reaction/400368
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | 2-Amino-5-phenyl-1,3,4-thiadiazole | HCID 219408 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-chloro-N-(5-phenyl-1,3,4-thiadiazol-2-yl)butanamide | HCID 8414075 | 85.2% |
Reaction Steps
A mixture of 5-phenyl-1,3,4-thiadiazol-2-amine (7.1 g, 0.04 mol), 4-chloro-butyryl chloride (11.3 g, 9.0 ml, 0.08 mol) and potassium carbonate (5.5 g, 0.04 mole) in toluene (100 ml) was heated under reflux for 4 hr. The toluene was then evaporated under reduced pressure. The residue was then quenched with water, stirred, and filtered. The solid obtained was washed, dried and recrystallized from toluene to give the required product (9.6 g, 85% yield), mp 159-62° C., m/e 281, 87% (consistent with molecular formula C12H12ClN3OS, calcd. 281.04). 1H NMR (DMSO-d6): δ 2.07-2.10 (m, 2H, —CH2), 2.67-2.70 (m, 2H, —CH2), 3.70-3.72 (m, 2H, —CH2), 7.48-7.54 (m, 3H, ArH), 7.93-7.94 (m, 2H, ArH), 12.65 (br s, 1H, NH). 13C NMR: δ 27.9, 32.7, 45.1, 127.4, 129.8, 130.7, 131.0, 158.5, 162.4, 171.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741893B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-220eb16f95bd44ad8f5201597c5e3588 |
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| Source note | uspto-grants-2014_06 |
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