HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220681Generated: October 31, 2026
Benzyltrimethylammonium hydroxide → HCID 370270, compound
https://huagongshe.com/reaction/2220681
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | 1,2-Bis(4-methylphenyl)-1,2-ethanedione | HCID 76996 | — |
| Reactant | 1,3-Bis(4-methylphenyl)propan-2-one | HCID 12420214 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 370270 | HCID 370270 | — |
Reaction Steps
23.13 g (0.11 mol) of 1,3-bis(p-tolyl)-2-propanone and 26.2 g (0.11 mol) of 4,4′-dimethylbenzil were dissolved in 75 ml of hot ethanol (abs.). 53 ml of a methanolic benzyltrimethylammonium hydroxide solution (0.11 mol Triton B, 35% Fluka) were slowly added dropwise at 80° C. with stirring (caution: the reaction batch froths vigorously) and refluxing was effected for 25 minutes. The crude product was filtered off after three hours, then washed with cold ethanol and recrystallized from toluene (violet red, yield: 46.2 g (95%); m.p.: 244-245° C., literature: 250.4-251.4° C. [15]; elemental analysis for C33H38O: found: C, 89.8%, H, 6.6%. calculated: C, 89.96%, H, 6.41%, MS-El [m/z (rel. intensity): M+440 (100), 412 (47), 206 (98), 191 (16), 189 (10)). The IR spectrum of 1,2,3,4-tetra(p-tolyl)cyclopenta-1,3-dien-5-one is shown in FIG. 10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07417247B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-31efafc87f324f3991366b5227a41a6d |
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| Source note | uspto-grants-2008_08 |
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