HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768669Generated: November 1, 2026
Potassium hydride → 4-(2,2-dimethyl-1-oxopropyl)-N-[4-(2,2-dimethyl-1-oxopropyl)-benzoyl]benzamide
https://huagongshe.com/reaction/1768669
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | 4-(2,2-Dimethyl-1-oxopropyl)-benzamide | HCID 10536234 | — |
| Reactant | Benzoyl chloride, 4-(2,2-dimethyl-1-oxopropyl)- | HCID 11806342 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(2,2-dimethyl-1-oxopropyl)-N-[4-(2,2-dimethyl-1-oxopropyl)-benzoyl]benzamide | HCID 9800724 | — |
Reaction Steps
4.2 grams (20.5 mmoles) of 4-(2,2-dimethyl-1-oxopropyl) benzamide is dissolved in 100 milliliters of dry tetrahydrofuran. The solution is cooled to 0° C., and 3.7 grams (22.6 mmoles) of potassium hydride (from a 24.5% mixture in mineral oil) which has been washed free of oil with hexane, is added. After hydrogen evolution has ceased, (approximately 2 hours), a solution of 4.6 grams (20.5 mmoles) of 4-(2,2-dimethyl-1-oxopropyl)-benzoyl chloride in 20 milliliters of dry tetrahydrofuran is added dropwise at 0° C. When addition is complete, the reaction mixture is concentrated in vacuo, and the residue is then dissolved in methylene dichloride and filtered to remove solids. The filtrate is purified by flash chromatography (3 inch column and 0.3% then 1% methanol/methylene chloride to elute) and crystallized from diethyl ether to yield the title product (m.p. 131°-132° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05378728 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-c881b126b3004ca1929902fc5ee5105c |
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| Source note | uspto-grants-1995_01 |
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